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Diisopropylethylamine → HCID 23554371、化合物

HRID 1859846
ノート
印刷プレビュー

反応式

HRID 1859846 の反応式
C1C=[C:5]2N=N[N:9](O)[C:4]2=[CH:3]C=1.[OH2:11].C(N(C(C)C)CC)(C)C.Cl.CN(C)CCCN=C=NCC.[NH2:33][CH:34]1[N:40]=[C:39]([C:41]2[CH:46]=[CH:45][CH:44]=[CH:43][N:42]=2)[C:38]2[CH:47]=[CH:48][CH:49]=[CH:50][C:37]=2[N:36]([CH2:51][C:52](=[O:57])[C:53]([CH3:56])([CH3:55])[CH3:54])[C:35]1=[O:58]>C(Cl)Cl>[NH2:9][C@H:4]([C:3]([NH:33][CH:34]1[N:40]=[C:39]([C:41]2[CH:46]=[CH:45][CH:44]=[CH:43][N:42]=2)[C:38]2[CH:47]=[CH:48][CH:49]=[CH:50][C:37]=2[N:36]([CH2:51][C:52](=[O:57])[C:53]([CH3:54])([CH3:55])[CH3:56])[C:35]1=[O:58])=[O:11])[CH3:5]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 81531DiisopropylethylamineHCID 27239391,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 27960291-Hydroxybenzotriazole hydrateHCID 10498048(3RS)-Amino-1-(tert-butylcarbonylmethyl)-2,3-dihydro-5-(2-pyridyl)-1H-1,4-benzodiazepin-2-one

生成物 1

HCID 23554371HCID 23554371、化合物収率 96%

試薬・触媒・溶媒

1
HCID 6344Dichloromethane溶媒2 回

実験手順

A solution of L-Boc-alanine (1.57 g, 8.33 mmol), HOBt monohydrate (1.13 g, 8.33 mmol), diisopropylethylamine (1.45 mL, 8.33 mmol) and CH2Cl2 (40 mL) was purged with nitrogen and cooled in an ice bath. To the cold solution was added 1-(3-dimethylaminopropyl)-3-ethylcarbodimide hydrochloride (1.60 g, 8.33 mmol) followed by a solution of 3-amino-2,3-dihydro-1-(3,3-dimethyl-2-oxobutyl)-5-(2-pyridyl)-1H-1,4-benzodiazepin-2-one (2.92 g, 8.33 mmol) dissolved in CH2Cl2 (25 mL). The cold bath was removed and the solution stirred overnight at room temperature. The reaction mixture was extracted with H2O, 0.1 N aq. citric acid, 5% aq. NaHCO3, and brine. The remaining CH2Cl2 solution was dried (MgSO4) and concentrated to a yellow foam. The title compound was isolated via column chromatography (20% EtOAc/hexanes to 60% EtOAc/hexanes) to give 4.19 g (96% yield) of light yellow foam.

後処理

  1. temperaturecooled in an ice bath
  2. customThe cold bath was removed
  3. extractionThe reaction mixture was extracted with H2O, 0.1 N aq. citric acid, 5% aq. NaHCO3, and brine
  4. dry with materialThe remaining CH2Cl2 solution was dried (MgSO4)
  5. concentrationconcentrated to a yellow foam

出典と根拠

ORDレコード
ord-1eb41cc1b9f8470b83967dcbd27b32b3
出典データセット
uspto-grants-2003_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06528505B1

反応ノート

読み込み中…

このページの内容参加物実験手順後処理出典と根拠反応ノート