Diisopropylethylamine → 4-diphenylcarbamoyl-1-pentyl(phenyl)carbamoyl-(2S)-hexahydro-2-pyrazinecarboxylic acid

HRID 2226599ノート

反応式

HRID 2226599 の反応式
C(O)(=O)C.[C:5]1([N:11]([C:23]2[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=2)[C:12]([N:14]2[CH2:19][CH2:18][NH:17][C@H:16]([C:20]([OH:22])=[O:21])[CH2:15]2)=[O:13])[CH:10]=[CH:9][CH:8]=[CH:7][CH:6]=1.C(N(CC)C(C)C)(C)C.[CH2:38]([N:43]([C:47]1[CH:52]=[CH:51][CH:50]=[CH:49][CH:48]=1)[C:44](Cl)=[O:45])[CH2:39][CH2:40][CH2:41][CH3:42]>CN(C=O)C>[CH2:38]([N:43]([C:47]1[CH:48]=[CH:49][CH:50]=[CH:51][CH:52]=1)[C:44]([N:17]1[CH2:18][CH2:19][N:14]([C:12](=[O:13])[N:11]([C:5]2[CH:6]=[CH:7][CH:8]=[CH:9][CH:10]=2)[C:23]2[CH:24]=[CH:25][CH:26]=[CH:27][CH:28]=2)[CH2:15][C@H:16]1[C:20]([OH:22])=[O:21])=[O:45])[CH2:39][CH2:40][CH2:41][CH3:42]

参加物

5

反応物 3

HCID 81531DiisopropylethylamineHCID 18965165N-pentyl-N-phenylcarbamoyl chlorideHCID 70074389(S)-4-(Diphenylcarbamoyl)piperazine-2-carboxylic acid acetate Salt

生成物 1

HCID 443038594-diphenylcarbamoyl-1-pentyl(phenyl)carbamoyl-(2S)-hexahydro-2-pyrazinecarboxylic acid

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

反応条件

温度
25 °C

実験手順

A stirred solution of 0.383 g (1.00 mmole) of (S)-4-(diphenylcarbamoyl)piperazine-2-carboxylic acid acetate salt (from Step C) and 0.400 g (3.09 mmole) of N,N-diisopropylethylamine in 6 ml of DMF at 0° C. was treated with 0.253 g (1.12 mmole) of N-pentyl-N-phenylcarbamoyl chloride (from Step B) and then was warmed to 25° C. for 16 hours. The DMF was removed in vacuo and the residue was partitioned between 20 ml of 1N HCl and 50 ml of chloroform which was dried over sodium sulfate and concentrated in vacuo to a yellow oil. The oil was flash chromatographed over 100 cc of silica gel with 12×25 ml of chloroform, 10×25 ml of 80:20:2 chloroform-methanol-ammonia water. Fractions 19-26 were combined and concentrated to 0.338 g (ammonium salt) of clear glass which was homogeneous by TLC (80:20:2 chloroform-methanol-ammonia water, Rf =0.4). The product was partitioned between 20 ml. of 1N HCl and 30 ml of chloroform which was dried over sodium sulfate and concentrated in vacuo to 0.337 g (72%) of a clear glass.

後処理

  1. customThe DMF was removed in vacuo
  2. customthe residue was partitioned between 20 ml of 1N HCl and 50 ml of chloroform which
  3. dry with materialwas dried over sodium sulfate
  4. concentrationconcentrated in vacuo to a yellow oil
  5. customchromatographed over 100 cc of silica gel with 12×25 ml of chloroform, 10×25 ml of 80:20:2 chloroform-methanol-ammonia water
  6. concentrationconcentrated to 0.338 g (ammonium salt) of clear glass which
  7. customThe product was partitioned between 20 ml
  8. dry with materialof 1N HCl and 30 ml of chloroform which was dried over sodium sulfate
  9. concentrationconcentrated in vacuo to 0.337 g (72%) of a clear glass

出典と根拠

ORDレコード
ord-8d0ff148d0db408ab0d307aab131ee38
出典データセット
uspto-grants-1994_09
特許番号
US05348955

反応ノート

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