Triethylamine → benzyl (3R)-4-(5-cyano-2-iodophenoxy)-3-(4-cyanobenzoylamino)butanoate

HRID 747768ノート

反応式

HRID 747768 の反応式
[Cl-].[CH2:2]([O:9][C:10]([CH2:12][C@@H:13]([NH3+:25])[CH2:14][O:15][C:16]1[CH:21]=[C:20]([C:22]#[N:23])[CH:19]=[CH:18][C:17]=1[I:24])=[O:11])[C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1.[C:26]([C:28]1[CH:36]=[CH:35][C:31]([C:32](O)=[O:33])=[CH:30][CH:29]=1)#[N:27].ON1C2C=CC=CC=2N=N1.C(N(CC)CC)C.Cl.CN(C)CCCN=C=NCC>ClCCl.O>[C:22]([C:20]1[CH:19]=[CH:18][C:17]([I:24])=[C:16]([CH:21]=1)[O:15][CH2:14][C@H:13]([NH:25][C:32](=[O:33])[C:31]1[CH:35]=[CH:36][C:28]([C:26]#[N:27])=[CH:29][CH:30]=1)[CH2:12][C:10]([O:9][CH2:2][C:3]1[CH:4]=[CH:5][CH:6]=[CH:7][CH:8]=1)=[O:11])#[N:23]

参加物

8

実験手順

4.73 g (10 mmol) of (1R)-1-benzyloxycarbonylmethyl-2-(5-cyano-2-iodophenoxy)ethylammonium chloride, 2.9 g (20 mmol) of 4-cyanobenzoic acid, 3.0 g (22 mmol) of 1-hydroxybenzotriazole and 6.1 ml (44 mmol) of triethylamine were dissolved in 50 ml of dichloromethane. 4.2 g (22 mmol) of 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride was added to the solution under cooling with ice, and they were stirred for 10 minutes and then at room temperature for one hour. Water is added to the reaction mixture to terminate the reaction. The mixture was treated with dichloromethane as the extractant in an ordinary manner to obtain the crude product, which was purified by the silica gel column chromatography (volume ratio of hexane:ethyl acetate=3:1) to obtain the title compound.

後処理

  1. temperatureunder cooling with ice, and they
  2. waitat room temperature for one hour
  3. customto terminate
  4. customthe reaction
  5. customto obtain the crude product, which
  6. customwas purified by the silica gel column chromatography (volume ratio of hexane:ethyl acetate=3:1)

出典と根拠

ORDレコード
ord-0ce0e02527c842c7999849f0faed2d91
出典データセット
uspto-grants-2008_07
特許番号
US07396844B1

反応ノート

読み込み中…