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Dichloromethane methanol → 4-(4-Amino-isoquinolin-1-yloxy)-piperidine-1-carboxylic acid tert-butyl ester

HRID 729608
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HRID 729608 반응식
[C:1]([O:5][C:6]([N:8]1[CH2:13][CH2:12][CH:11]([O:14][C:15]2[C:24]3[C:19](=[CH:20][CH:21]=[CH:22][CH:23]=3)[C:18]([N+:25]([O-])=O)=[CH:17][N:16]=2)[CH2:10][CH2:9]1)=[O:7])([CH3:4])([CH3:3])[CH3:2].CO.ClCCl>C1COCC1.C(O)C.[Pd]>[C:1]([O:5][C:6]([N:8]1[CH2:9][CH2:10][CH:11]([O:14][C:15]2[C:24]3[C:19](=[CH:20][CH:21]=[CH:22][CH:23]=3)[C:18]([NH2:25])=[CH:17][N:16]=2)[CH2:12][CH2:13]1)=[O:7])([CH3:4])([CH3:2])[CH3:3]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 2

HCID 21226129Dichloromethane methanolHCID 69053768HCID 69053768, 화합물

생성물 1

HCID 578328234-(4-Amino-isoquinolin-1-yloxy)-piperidine-1-carboxylic acid tert-butyl ester수율 98.4%

시약·촉매·용매 3

HCID 23938Palladium촉매HCID 702Ethanol용매2회
HCID 8028
Tetrahydrofuran
용매

실험 절차

To a slurry of 4-(4-nitro-isoquinolin-1-yloxy)-piperidine-1-carboxylic acid tert-butyl ester (33.5 g, 89.7 mmol) in THF (300 mL) and ethanol (300 mL) add 10% Pd/C (1.80 g, 1.69 mmol) as a slurry in ethanol (25 mL). Place the mixture in a Parr shaker under hydrogen atmosphere (25-40 psi) at room temperature for 8 hours. Filter the mixture through a pad of diatomaceous earth and wash with ethanol until the filtrate is colorless. Concentrate the filtrate under reduced pressure to give dark oil. Subject residue to silica gel chromatography eluting with 1% then 2.5% MeOH/dichloromethane to afford the title compound (30.3 g, 98% yield) as an orange glass. (ES+): m/z 344 (M++H).

후처리

  1. customat room temperature
  2. customfor 8 hours
  3. filtrationFilter the mixture through a pad of diatomaceous earth
  4. washwash with ethanol until the filtrate
  5. concentrationConcentrate the filtrate under reduced pressure
  6. customto give dark oil
  7. washSubject residue to silica gel chromatography eluting with 1%

출처 및 근거

ORD 기록
ord-3bc3165130b74abda4c7201d6843e3aa
출처 데이터셋
uspto-grants-2009_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07582638B2

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