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Cyclopropanecarboxylic acid → Cyclopropyl-[4-(4-nitro-isoquinolin-1-yl)-piperazin-1-yl]-methanone

HRID 729614
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HRID 729614 반응식
[N+:1]([C:4]1[C:13]2[C:8](=[CH:9][CH:10]=[CH:11][CH:12]=2)[C:7]([N:14]2[CH2:19][CH2:18][NH:17][CH2:16][CH2:15]2)=[N:6][CH:5]=1)([O-:3])=[O:2].[CH:20]1([C:23](O)=[O:24])[CH2:22][CH2:21]1.CCN=C=NCCCN(C)C>CN(C1C=CN=CC=1)C.ClCCl>[CH:20]1([C:23]([N:17]2[CH2:16][CH2:15][N:14]([C:7]3[C:8]4[C:13](=[CH:12][CH:11]=[CH:10][CH:9]=4)[C:4]([N+:1]([O-:3])=[O:2])=[CH:5][N:6]=3)[CH2:19][CH2:18]2)=[O:24])[CH2:22][CH2:21]1
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참가 물질

6

반응물 3

HCID 15655Cyclopropanecarboxylic acidHCID 159081-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 578328074-Nitro-1-piperazin-1-yl-isoquinoline

생성물 1

HCID 57832816Cyclopropyl-[4-(4-nitro-isoquinolin-1-yl)-piperazin-1-yl]-methanone수율 79%

시약·촉매·용매 2

HCID 142844-(Dimethylamino)pyridine촉매
HCID 6344
Dichloromethane
용매

실험 절차

Treat a solution or slurry of 4-nitro-1-piperazin-1-yl-isoquinoline (Preparation 26, 517 mg, 2 mmol), cyclopropanecarboxylic acid (258 mg, 3 mmol) and catalytic DMAP (24 mg, 0.2 mmol) in dichloromethane (20 mL) with EDCI (575 mg, 3 mmol). Agitate the resulting mixture at ambient temperature overnight, then wash with saturated aqueous sodium bicarbonate solution. Dry the organic layer over sodium sulfate and concentrate under reduced pressure. Subject residue to silica gel chromatography using a gradient of 0-2% 2M ammonia-methanol in dichloromethane and a gradient of 0-70% ethyl acetate in hexanes to give a yellow solid after two purifications. (513 mg, 79% yield, LCMS ES+ (m/z) 327 [M+H]).

후처리

  1. washwash with saturated aqueous sodium bicarbonate solution
  2. dry with materialDry the organic layer over sodium sulfate
  3. concentrationconcentrate under reduced pressure
  4. customa gradient of 0-70% ethyl acetate in hexanes to give a yellow solid after two purifications

출처 및 근거

ORD 기록
ord-fa1cd912677440fb9bb9a1bfb6c4050e
출처 데이터셋
uspto-grants-2009_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07582638B2

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