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Boc-Ala-Gly-Gly-OBzl → Boc-ala-Gly-Gly-OH

HRID 1379603
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HRID 1379603 반응식
[NH:1]([C:22]([O:24][C:25]([CH3:28])([CH3:27])[CH3:26])=[O:23])[C@H:2]([C:4]([NH:6][CH2:7][C:8]([NH:10][CH2:11][C:12]([O:14]CC1C=CC=CC=1)=[O:13])=[O:9])=[O:5])[CH3:3]>C(O)C.[Pd]>[NH:1]([C:22]([O:24][C:25]([CH3:26])([CH3:28])[CH3:27])=[O:23])[C@H:2]([C:4]([NH:6][CH2:7][C:8]([NH:10][CH2:11][C:12]([OH:14])=[O:13])=[O:9])=[O:5])[CH3:3]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 131720212Boc-Ala-Gly-Gly-OBzl

생성물 1

HCID 7020897Boc-ala-Gly-Gly-OH

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 702Ethanol용매

실험 절차

0.5 g (1.3 mmol) of Boc-Ala-Gly-Gly-OBzl (13) is dissolved in 25 ml of absolute ethanol (Aldrich) in a 50 ml round bottom flask equipped with a stirring bar, followed by addition of 50 mg of 10% Pd-C (Aldrich). The reaction mixture is stirred under hydrogen gas atmosphere using a balloon. After 24 h, the Pd-C catalyst is filtered out from the reaction mixture, and the filtrate is concentrated to furnish Boc-Ala-Gly-Gly-OH (14). 1H-NMR (CDCl3): 1.39 (3H, d, J=7.2 Hz), 1.43 (9H, s), 3.99-4.15 (5H, m), 5.03 (1H, br), 6.91-7.03 (2H, br). FABMS: 325 (M+Na).

후처리

  1. customequipped with a stirring bar
  2. filtrationthe Pd-C catalyst is filtered out from the reaction mixture
  3. concentrationthe filtrate is concentrated

출처 및 근거

ORD 기록
ord-b2b1565f1401459b8a69642d22d5eace
출처 데이터셋
uspto-grants-1997_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05672584

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