反応 #4122169
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-679142328dbc4a2aa9ca3dd30d602461表示可能な構造データがありません
C1CN(CCN1)C(=O)C(F)(F)F製品情報
2,2,2-trifluoro-1-piperazin-1-ylethanone (CAS 6511-88-2) 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 7172020
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-679142328dbc4a2aa9ca3dd30d602461反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-ca83c8394b304fcd837006880c05bda9反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: To a solution of compound 1c (15.15 g, 53.69 mmol) in CH2Cl2 (60 mL) was added trifluoroacetic acid (18 mL) at room temperature. The mixture was stirred at room temperature for 18 h. The solvent was removed by evaporation. Ether (100 mL) was added to the residue. The white solid was collected by filtration, washed with ether, and dried under vacuum. The crude compound 1d was used in the next reaction without further purification. MS m/z (M+H+) 183.1. The solvent was removed by evaporation Ether (100 mL) was added to the residue The white solid was collected by filtration washed with ether dried under vacuum The crude compound 1d was used in the next reaction without further purification
ソース ID: ord-13a94fe105ab43799c4b132dee85e047反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: To a solution of compound 1c (15.15 g, 53.69 mmol) in CH2Cl2 (60 mL) was added trifluoroacetic acid (18 mL) at room temperature. The mixture was stirred at room temperature for 18 h. The solvent was removed by evaporation. Ether (100 mL) was added to the residue. The white solid was collected by filtration, washed with ether, and dried under vacuum. The crude compound 1d was used in the next reaction without further purification. MS m/z (M+H+) 183.1. The solvent was removed by evaporation Ether (100 mL) was added to the residue The white solid was collected by filtration washed with ether dried under vacuum The crude compound 1d was used in the next reaction without further purification
ソース ID: ord-ded4dd7687d24841bd7e0c839e07469f反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: To a solution of compound 1c (15.15 g, 53.69 mmol) in CH2Cl2 (60 mL) was added trifluoroacetic acid (18 mL) at room temperature. The mixture was stirred at room temperature for 18 h. The solvent was removed by evaporation. Ether (100 mL) was added to the residue. The white solid was collected by filtration, washed with ether, and dried under vacuum. The crude compound 1d was used in the next reaction without further purification. MS m/z (M+H+) 183.1. The solvent was removed by evaporation Ether (100 mL) was added to the residue The white solid was collected by filtration washed with ether dried under vacuum The crude compound 1d was used in the next reaction without further purification
ソース ID: ord-ded4dd7687d24841bd7e0c839e07469f反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: Following Example 216, to a well stirred solution of 8-(1H-Pyrazol-4-yl)-4,5-dihydro-6-oxa-3-thia-1-aza-benzo[e]azulene-2-carboxylic acid and 2,2,2-trifluoro-1-(piperazin-1-yl)ethanone to give 229. MS: (ESI+)=478.1
ソース ID: ord-fe1e475dbfb24683b1811c9980cf80ba反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: Following Example 216, to a well stirred solution of 8-(1H-Pyrazol-4-yl)-4,5-dihydro-6-oxa-3-thia-1-aza-benzo[e]azulene-2-carboxylic acid and 2,2,2-trifluoro-1-(piperazin-1-yl)ethanone to give 229. MS: (ESI+)=478.1
ソース ID: ord-fe1e475dbfb24683b1811c9980cf80ba反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: To a solution of compound 1c (15.15 g, 53.69 mmol) in CH2Cl2 (60 mL) was added trifluoroacetic acid (18 mL) at room temperature. The mixture was stirred at room temperature for 18 h. The solvent was removed by evaporation. Ether (100 mL) was added to the residue. The white solid was collected by filtration, washed with ether, and dried under vacuum. The crude compound 1d was used in the next reaction without further purification. MS m/z (M+H+) 183.1. The solvent was removed by evaporation Ether (100 mL) was added to the residue The white solid was collected by filtration washed with ether dried under vacuum The crude compound 1d was used in the next reaction without further purification
ソース ID: ord-73ee6f5c369b4d6fbb6c6fce896620b0反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: To a solution of compound 1c (15.15 g, 53.69 mmol) in CH2Cl2 (60 mL) was added trifluoroacetic acid (18 mL) at room temperature. The mixture was stirred at room temperature for 18 h. The solvent was removed by evaporation. Ether (100 mL) was added to the residue. The white solid was collected by filtration, washed with ether, and dried under vacuum. The crude compound 1d was used in the next reaction without further purification. MS m/z (M+H+) 183.1. The solvent was removed by evaporation Ether (100 mL) was added to the residue The white solid was collected by filtration washed with ether dried under vacuum The crude compound 1d was used in the next reaction without further purification
ソース ID: ord-73ee6f5c369b4d6fbb6c6fce896620b0反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: To a solution of compound 1c (15.15 g, 53.69 mmol) in CH2Cl2 (60 mL) was added trifluoroacetic acid (18 mL) at room temperature. The mixture was stirred at room temperature for 18 h. The solvent was removed by evaporation. Ether (100 mL) was added to the residue. The white solid was collected by filtration, washed with ether, and dried under vacuum. The crude compound 1d was used in the next reaction without further purification. MS m/z (M+H+) 183.1. The solvent was removed by evaporation Ether (100 mL) was added to the residue The white solid was collected by filtration washed with ether dried under vacuum The crude compound 1d was used in the next reaction without further purification
ソース ID: ord-13a94fe105ab43799c4b132dee85e047反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: To a solution of compound 1c (15.15 g, 53.69 mmol) in CH2Cl2 (60 mL) was added trifluoroacetic acid (18 mL) at room temperature. The mixture was stirred at room temperature for 18 h. The solvent was removed by evaporation. Ether (100 mL) was added to the residue. The white solid was collected by filtration, washed with ether, and dried under vacuum. The crude compound 1d was used in the next reaction without further purification. MS m/z (M+H+) 183.1. The solvent was removed by evaporation Ether (100 mL) was added to the residue The white solid was collected by filtration washed with ether dried under vacuum The crude compound 1d was used in the next reaction without further purification
ソース ID: ord-13a94fe105ab43799c4b132dee85e047反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: To a stirred solution of 2,2,2-trifluoro-1-piperazin-1-yl-ethanone (515 mg, 2.83 mmol) in dry CH3CN (6 mL) was added allyl bromide (0.32 mL, 3.7 mmol) and powdered potassium carbonate (0.78 g, 5.65 mmol) and the mixture stirred overnight. The reaction was concentrated under reduced pressure, diluted with CH2Cl2 (30 mL) and water (30 mL) and the aqueous layer extracted with CH2Cl2 (2×20 mL). The combined organic extracts were dried (Na2SO4), filtered and concentrated in vacuo to afford the crude di-protected piperazine (0.554 g) which was used without further purification in the next reaction. The reaction was concentrated under reduced pressure diluted with CH2Cl2 (30 mL) and water (30 mL) the aqueous layer extracted with CH2Cl2 (2×20 mL) The combined organic extracts were dried (Na2SO4) filtered concentrated in vacuo
ソース ID: ord-32ee4c940d754b23bf862be162c61ba9PubChem 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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