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Methanol → 2-(Aminosulfonylamino)pentanoic acid methyl ester

HRID 1289622
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인쇄 미리보기

반응식

HRID 1289622 반응식
C([NH:11][S:12]([NH:15][CH:16]([CH2:20][CH2:21][CH3:22])[C:17]([OH:19])=[O:18])(=[O:14])=[O:13])(OCC1C=CC=CC=1)=O.[CH3:23]O>[Pd]>[CH3:23][O:19][C:17](=[O:18])[CH:16]([NH:15][S:12]([NH2:11])(=[O:14])=[O:13])[CH2:20][CH2:21][CH3:22]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 887MethanolHCID 189222562-(N-carbobenzyloxyaminosulfonyl)aminopentanoic acid

생성물 1

HCID 539168252-(Aminosulfonylamino)pentanoic acid methyl ester수율 90%

시약·촉매·용매 1

HCID 23938Palladium촉매

실험 절차

A mixture of 2-(N-carbobenzyloxyaminosulfonyl)aminopentanoic acid (46.7 g), methanol (350 mL) and 10% palladium on carbon (3.0 g) was hydrogenated at 55 psi for about 2 hours. The catalyst was removed by filtration through CELITE®, the solvent was removed in vacuo and the residue was purified by column chromatography on silica eluting with 50% ethyl acetate/hexane to afford 25.6 g (90%) of 2-(aminosulfonylamino)pentanoic acid methyl ester (Formula V: R=CH3 ; R1 =propyl; R2 =H; R3 =H), m.p. 63°-64° C.

후처리

  1. customThe catalyst was removed by filtration through CELITE®
  2. customthe solvent was removed in vacuo
  3. customthe residue was purified by column chromatography on silica eluting with 50% ethyl acetate/hexane

출처 및 근거

ORD 기록
ord-ff6a248b0c284366b26da0c5aff681d4
출처 데이터셋
uspto-grants-1998_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05750546

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