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N-(carbobenzyloxyaminosulfonyl)-2-propyl-DL-alanine methyl ester → N-aminosulfonyl-2-propyl-DL-alanine methyl ester

HRID 743449
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인쇄 미리보기

반응식

HRID 743449 반응식
[CH3:1][O:2][C:3](=[O:24])[C:4]([CH2:21][CH2:22][CH3:23])([CH3:20])[NH:5][S:6]([NH:9]C(OCC1C=CC=CC=1)=O)(=[O:8])=[O:7]>[Pd].CO>[CH3:1][O:2][C:3](=[O:24])[C:4]([CH2:21][CH2:22][CH3:23])([CH3:20])[NH:5][S:6]([NH2:9])(=[O:7])=[O:8]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 19424434N-(carbobenzyloxyaminosulfonyl)-2-propyl-DL-alanine methyl ester

생성물 1

HCID 19424444N-aminosulfonyl-2-propyl-DL-alanine methyl ester수율 79.8%

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 887Methanol용매

실험 절차

A mixture of N-(carbobenzyloxyaminosulfonyl)-2-propyl-DL-alanine methyl ester (22.35 g, 62.36 mmol), methanol (200 mL) and 10% palladium on Carbon (1.0 g) was placed on a Parr hydrogenator at 60 psi for 1.5 hours. The reaction mixture was passed through a pad of CELITE®, and the filtrate was concentrated in vacuo to afford 11.16 g (79.8%) of N-aminosulfonyl-2-propyl-DL-alanine methyl ester (Formula VII: R=CH3 ; R1 =propyl; R2 =CH3; R3 =H).

후처리

  1. concentrationthe filtrate was concentrated in vacuo

출처 및 근거

ORD 기록
ord-a54e83a07a394a24b675c8886c85f1c9
출처 데이터셋
uspto-grants-1996_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05556909

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