tert-butyl N-(4-aminobutyl)carbamate → {4-[3-({2-[(4-Cyano-phenylamino)-methyl]-1-methyl-1H-benzoimidazole-5-carbonyl}-phenyl-amino)-propionylamino]-butyl}-carbamic acid tert-butyl ester

HRID 68189

反応式

HRID 68189 の反応式
[C:1]([C:3]1[CH:8]=[CH:7][C:6]([NH:9][CH2:10][C:11]2[N:15]([CH3:16])[C:14]3[CH:17]=[CH:18][C:19]([C:21]([N:23]([C:29]4[CH:34]=[CH:33][CH:32]=[CH:31][CH:30]=4)[CH2:24][CH2:25][C:26](O)=[O:27])=[O:22])=[CH:20][C:13]=3[N:12]=2)=[CH:5][CH:4]=1)#[N:2].F[B-](F)(F)F.N1(OC(N(C)C)=[N+](C)C)C2C=CC=CC=2N=N1.CN1CCOCC1.[C:64]([O:68][C:69](=[O:76])[NH:70][CH2:71][CH2:72][CH2:73][CH2:74][NH2:75])([CH3:67])([CH3:66])[CH3:65]>CN(C=O)C.O.C(OCC)(=O)C>[C:64]([O:68][C:69](=[O:76])[NH:70][CH2:71][CH2:72][CH2:73][CH2:74][NH:75][C:26](=[O:27])[CH2:25][CH2:24][N:23]([C:21]([C:19]1[CH:18]=[CH:17][C:14]2[N:15]([CH3:16])[C:11]([CH2:10][NH:9][C:6]3[CH:5]=[CH:4][C:3]([C:1]#[N:2])=[CH:8][CH:7]=3)=[N:12][C:13]=2[CH:20]=1)=[O:22])[C:29]1[CH:34]=[CH:33][CH:32]=[CH:31][CH:30]=1)([CH3:67])([CH3:65])[CH3:66]

参加物

8

実験手順

A solution of the product of 1e (5.23 mmol), 2-(1H-benzotriazole-1-yl)-1,1,3,3-tetramethyluronium tetrafluoroborate (TBTU, 5.23 mmol) and N-methyl-morpholin (5.23 mmol) in 20 mL DMF was stirred at room temperature for 30 minutes. Then (4-amino-butyl)-carbamic acid tert-butyl ester (5.23 mmol) was added and the mixture stirred at room temperature for another 24 hours. The mixture was then diluted with water (100 mL) and the product was isolated through extraction with ethyl acetate.

出典と根拠

ORDレコード
ord-62aca8cd28694b80a8c88a8665d54cf6
出典データセット
uspto-grants-2014_09
特許番号
US08821871B2

関連ノート

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