反応 #4077448
関連文献 (1)
openreactiondata ↗doi:10.1039/C8SC04228D
反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-310398e0e3284e6394830cb2880e4b45表示可能な構造データがありません
C1=CC=C(C=C1)COC(=O)NCCNCCNC(=O)OCC2=CC=CC=C2化学中間体
構造・識別子・計算物性は CAS によりデータベース記録と照合済みです。
| 中間体 | benzyl N-[2-[2-(phenylmethoxycarbonylamino)ethylamino]ethyl]carbamate |
|---|---|
| IUPAC 名 | — |
| CAS番号 | 160256-75-7 |
| データベース ID | 4367374 |
| 分子式 | — |
| 分子量 | — |
製品情報
benzyl N-[2-[2-(phenylmethoxycarbonylamino)ethylamino]ethyl]carbamate (CAS 160256-75-7) product identity, structure identifiers and related reaction data for chemical intermediate research and sourcing review.
想定用途
専門的研究・工業用途限定
データベース ID 4367374
安全上の注意
For professional research and industrial use only. Review the supplier safety data sheet before handling.
合成データ
12 反応 · 12 文献
反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-310398e0e3284e6394830cb2880e4b45反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 51.5 g (500 mmol) of diethylenetriamine and 139 ml (1 mol) of triethylamine are dissolved in dichloromethane and mixed at -20° C. with 161 g of benzyl cyanoformate (Fluka) in dichloromethane and then stirred overnight at room temperature. After the reaction is completed, concentration by evaporation is performed during draw-off, the residue is taken up in diethyl ether, the organic phase is washed with sodium carbonate solution and dried with sodium sulfate. The filtrate is mixed with hexane, the precipitate is filtered out and dried. concentration by evaporation the organic phase is washed with sodium carbonate solution dried with sodium sulfate The filtrate is mixed with hexane the precipitate is filtered out dried
ソース ID: ord-b8b16aaaca1e4eaeb10499e1d4ff9603反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 51.5 g (500 mmol) of diethylenetriamine and 139 ml (1 mol) of triethylamine are dissolved in dichloromethane and mixed at -20° C. with 161 g of benzyl cyanoformate (Fluka) in dichloromethane and then stirred overnight at room temperature. After the reaction is completed, concentration by evaporation is performed during draw-off, the residue is taken up in diethyl ether, the organic phase is washed with sodium carbonate solution and dried with sodium sulfate. The filtrate is mixed with hexane, the precipitate is filtered out and dried. concentration by evaporation the organic phase is washed with sodium carbonate solution dried with sodium sulfate The filtrate is mixed with hexane the precipitate is filtered out dried
ソース ID: ord-44d657dd93a14d4a9555e1b08402b1a6反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 5.15 g (50 mmol) of diethylenetriamine and 13.9 ml (100 mmol) of triethylamine are dissolved in dichloromethane and mixed at -20° C. with 16.1 g of benzyl cyanoformate (Fluka) in dichloromethane, and then it is stirred overnight at room temperature. After the reaction has been completed, it is evaporated during draw-off, the residue is taken up in diethyl ether, the organic phase is washed with sodium carbonate solution and dried with sodium sulfate. The filtrate is mixed with hexane, the precipitate is filtered off and dried. it is evaporated during draw-off, the residue the organic phase is washed with sodium carbonate solution dried with sodium sulfate The filtrate is mixed with hexane the precipitate is filtered off dried
ソース ID: ord-87bb300a9aba4cda989453046d17f2fe反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 51.5 g (500 mmol) of diethylenetriamine and 139 ml (1 mol) of triethylamine are dissolved in dichloromethane and mixed at -20° C. with 161 g of benzyl cyanoformate (Fluka) in dichloromethane and then stirred overnight at room temperature. After the reaction is completed, concentration by evaporation is performed during draw-off, the residue is taken up in diethyl ether, the organic phase is washed with sodium carbonate solution and dried with sodium sulfate. The filtrate is mixed with hexane, the precipitate is filtered out and dried. concentration by evaporation the organic phase is washed with sodium carbonate solution dried with sodium sulfate The filtrate is mixed with hexane the precipitate is filtered out dried
ソース ID: ord-8160045cfd184bfcaacb0d316101536f反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 51.5 g (500 mmol) of diethylenetriamine and 139 ml (1 mol) of triethylamine are dissolved in dichloromethane and mixed at -20° C. with 161 g of benzyl cyanoformate (Fluka) in dichloromethane and then stirred overnight at room temperature. After the reaction is completed, concentration by evaporation is performed during draw-off, the residue is taken up in diethyl ether, the organic phase is washed with sodium carbonate solution and dried with sodium sulfate. The filtrate is mixed with hexane, the precipitate is filtered out and dried. concentration by evaporation the organic phase is washed with sodium carbonate solution dried with sodium sulfate The filtrate is mixed with hexane the precipitate is filtered out dried
ソース ID: ord-8160045cfd184bfcaacb0d316101536f反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 51.5 g (500 mmol) of diethylenetriamine and 139 ml (1 mol) of triethylamine are dissolved in dichloromethane and mixed at -20° C. with 161 g of benzyl cyanoformate (Fluka) in dichloromethane and then stirred overnight at room temperature. After the reaction is completed, concentration by evaporation is performed during draw-off, the residue is taken up in diethyl ether, the organic phase is washed with sodium carbonate solution and dried with sodium sulfate. The filtrate is mixed with hexane, the precipitate is filtered off and dried. concentration by evaporation the organic phase is washed with sodium carbonate solution dried with sodium sulfate The filtrate is mixed with hexane the precipitate is filtered off dried
ソース ID: ord-5e8619984f7f4291b6708117eb00dc08反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 14.86 g (40 mmol) of the bis[2-(benzyloxycarbonylamino)-ethyl]-amine described in Example 1a and 20.24 g (200 mmol) of triethylamine are dissolved in dimethylformamide and mixed with 4.96 g (20 mmol) of 5-nitro-isophthalic acid dichloride (J. Chem. Soc. 1957, 1172-1175) and stirred overnight at room temperature. The solution is concentrated by evaporation in a vacuum and the residue is chromatographed with ethyl acetate on silica gel. The solution is concentrated by evaporation in a vacuum the residue is chromatographed with ethyl acetate on silica gel
ソース ID: ord-51fe1b4e2e1f42c685f7064504a78e2b反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 37.14 g (100 mmol) of the bis(benzyloxycarbonylaminoethyl)-amine described in Example 1a is dissolved in DMF, mixed in an ice bath with 17.4 g (150 mmol) of diglycolic anhydride (Janssen Chimica) and 21 ml (150 mmol) of triethylamine and then stirred overnight at room temperature. The solution is concentrated by evaporation in a vacuum, the residue is taken up in ethyl acetate and shaken out with diluted hydrochloric acid. The organic phase is dried with sodium sulfate and after filtration from drying agent, it is crystallized by adding hexane. The solution is concentrated by evaporation in a vacuum shaken out with diluted hydrochloric acid The organic phase is dried with sodium sulfate after filtration from drying agent, it is crystallized by adding hexane
ソース ID: ord-47f7d99797424acb961b5b03aec76798反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 51.5 g (500 mmol) of diethylenetriamine and 139 ml (1 mol) of triethylamine are dissolved in dichloromethane and mixed at −20° C. with 161 g of benzyl cyanoformate (Fluka) in dichloromethane and then stirred overnight at room temperature. After completion of the reaction, concentration by evaporation is performed during draw-off, the residue is taken up in diethyl ether, the organic phase is washed with sodium carbonate solution and dried with sodium sulfate. The filtrate is mixed with hexane, the precipitate is filtered off and dried. After completion of the reaction, concentration by evaporation the organic phase is washed with sodium carbonate solution dried with sodium sulfate The filtrate is mixed with hexane the precipitate is filtered off dried
ソース ID: ord-a661f4bf15364d70800b20b465097663反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 51.5 g (500 mmol) of diethylenetriamine and 139 ml (1 mol) of triethylamine are dissolved in dichloromethane and mixed at -20° C. with 161 g of benzyl cyanoformate (Fluka) in dichloromethane and then stirred overnight at room temperature. After the reaction is completed, concentration by evaporation is performed during draw-off, the residue is taken up in diethyl ether, the organic phase is washed with sodium carbonate solution and dried with sodium sulfate. The filtrate is mixed with hexane, and the precipitate is filtered off and dried. concentration by evaporation the organic phase is washed with sodium carbonate solution dried with sodium sulfate The filtrate is mixed with hexane the precipitate is filtered off dried
ソース ID: ord-45867621a1b947e884ec397565fda740反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 51.5 g (500 mmol) of diethylenetriamine and 139 ml (1 mol) of triethylamine are dissolved in dichloromethane and mixed at −20° C. with 161 g of benzyl cyanoformate (Fluka) in dichloromethane and then stirred overnight at room temperature. After the reaction is completed, concentration by evaporation is performed during draw-off, the residue is taken up in diethyl ether, the organic phase is washed with sodium carbonate solution and dried with sodium sulfate. The filtrate is mixed with hexane, the precipitate is filtered out and dried. concentration by evaporation the organic phase is washed with sodium carbonate solution dried with sodium sulfate The filtrate is mixed with hexane the precipitate is filtered out dried
ソース ID: ord-3249f66ea4404cfc92c0df7e7fd4690ePubChem References
化合物の公開データベース記録に掲載された情報源です。
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