反応 #4100670
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-bfcbc53423d741ff83aeb6a50da8650e表示可能な構造データがありません
CC(=N)N製品情報
ethanimidamide (CAS 143-37-3) 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 67171
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-bfcbc53423d741ff83aeb6a50da8650e反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-cab564f21e884a539f442cb21a117e14反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-8816b98763804fe98ce78b4332612fc1反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-b378e4c8c27c496a8c9cfa726d9b9a8a反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-a6e6c8075cb5446ca0c11b70d0086b4d反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-06f707977fcd4160b2ddef16639cc758反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: The α-methoxymethylene-β-formylaminopropionitrile solution and the acetamidine solution are combined. The mixture is reacted at 25°C for 10 minutes. The reaction mixture is subjected to concentration at not higher than 40°C to give crystals. The produced crystals are washed with 50 parts by volume of ethanol, whereby 24.8 parts of 2-methyl-4-amino-5-formylaminomethylpyrimidine is obtained as crystals (Purity: 93 %). The ethanol washing is concentrated to give 16 parts of 2-methyl-4-amino-5-formylaminomethylpyrimidine as crystals (Purity: 47.5 %). The mixture is reacted at 25°C for 10 minutes The reaction mixture is subjected to concentration at not higher than 40°C to give crystals The produced crystals are washed with 50 parts by volume of ethanol, whereby 24.8 parts of 2-methyl-4-amino-5-formylaminomethylpyrimidine is obtained as crystals (Purity: 93 %) The ethanol washing is concentrated
ソース ID: ord-ba9435c8b58f426881a6b2e81a6aeee9反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: Reaction of acetamidine with 2,6-dichlorostyrylsulfonyl chloride according to the procedure of Example 29 (b) affords N'-[(2,6-dichlorostyryl)sulfonyl]acetamidine, m.p. 154.5°-158.5° C. (corr.), from absolute ethanol.
ソース ID: ord-c048d0a4ec6d4d3f9fac6060feeec184反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: Reaction of acetamidine with 2-nitrostyrylsulfonyl chloride according to the above procedure affords N-(2-NITROSTYRYL-SULFONYL)ACETAMIDINE, m.p. 175°-178° C.
ソース ID: ord-bd2c14f2aba540e4b9a04d439fddc145反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: Reaction of acetamidine with 4-chlorostyrylsulfonyl chloride according to the above procedure affords N-[(4-CHLOROSTYRYL)-SULFONYL]ACETAMIDINE, m.p. 161°-163° C., crystallized from ethyl acetate.
ソース ID: ord-f5e9dc7859674915844b94b7b277315c反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: Reaction of actamidine with 3,4-dichlorostyrylsulfonyl chloride according to the above procedure affords N-[(3,4-DICHLOROSTYRYL)SULFONYL]ACETAMIDINE, m.p. 197.5°-198.5° C. (corr.), crystallized from acetone-isopropanol.
ソース ID: ord-dbd8b88664d14a4bbd0c7cdbc543cdd0反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: Reaction of acetamidine with 4-nitrostyrylsulfonyl chloride according to the above procedure provides N-(4-NITROSTYRYLSULFONYL)ACETAMIDINE, m.p. 203.0°-203.5° C. (dec.)(corr.), crystallized from acetonitrile.
ソース ID: ord-d2b23b8b12154118bf76e397b36aae0dPubChem 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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