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[(3,5-Bis-benzyloxy-pyridine-2-carbonyl)-amino]-acetic acid methyl ester → HCID 59030678, 화합물

HRID 1158564
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HRID 1158564 반응식
[CH3:1][O:2][C:3](=[O:30])[CH2:4][NH:5][C:6]([C:8]1[C:13]([O:14]CC2C=CC=CC=2)=[CH:12][C:11]([O:22]CC2C=CC=CC=2)=[CH:10][N:9]=1)=[O:7]>CO.[Pd]>[CH3:1][O:2][C:3](=[O:30])[CH2:4][NH:5][C:6]([C:8]1[C:13]([OH:14])=[CH:12][C:11]([OH:22])=[CH:10][N:9]=1)=[O:7]
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참가 물질

4

반응물 1

HCID 59030679[(3,5-Bis-benzyloxy-pyridine-2-carbonyl)-amino]-acetic acid methyl ester

생성물 1

HCID 59030678HCID 59030678, 화합물수율 100%

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 887Methanol용매

실험 절차

To a solution [(3,5-bis-benzyloxy-pyridine-2-carbonyl)-amino]-acetic acid methyl ester (3.50 g, 8.62 mmol) in MeOH (100 mL) is added 10% Pd/C (0.350 g, 0.862 mmol) and the reaction mixture stirred under an atmosphere of H2 at room temperature for 16 hours. The suspension is filtered through Celite™ and the filtrate concentrated under reduced pressure. The crude material is purified over silica (MeOH:CH2Cl2 gradient 1% to 5%) to afford 1.95 g (quantitative yield) of the desired compound as an off-white solid. 1H NMR (250 MHz, MeOD) δ ppm 7.62 (1H, d, J=2.4 Hz), 6.53 (1H, d, J=2.4 Hz), 4.04 (2H, s), 3.64 (3H, s). HPLC-MS: m/z 227 [M+H]+.

후처리

  1. filtrationThe suspension is filtered through Celite™
  2. concentrationthe filtrate concentrated under reduced pressure
  3. customThe crude material is purified over silica (MeOH:CH2Cl2 gradient 1% to 5%)

출처 및 근거

ORD 기록
ord-b510a76df237417dbab040be46ff5f21
출처 데이터셋
uspto-grants-2010_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07811595B2

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