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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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1-Methanesulfonyl-piperidine-4-carboxylic acid benzyl ester → 1-Methanesulfonylpiperidine-4-carboxylic acid

HRID 589329
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인쇄 미리보기

반응식

HRID 589329 반응식
C([O:8][C:9]([CH:11]1[CH2:16][CH2:15][N:14]([S:17]([CH3:20])(=[O:19])=[O:18])[CH2:13][CH2:12]1)=[O:10])C1C=CC=CC=1>C(OCC)(=O)C.CO.[Pd]>[CH3:20][S:17]([N:14]1[CH2:15][CH2:16][CH:11]([C:9]([OH:10])=[O:8])[CH2:12][CH2:13]1)(=[O:19])=[O:18]
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참가 물질

5

반응물 1

HCID 574280631-Methanesulfonyl-piperidine-4-carboxylic acid benzyl ester

생성물 1

HCID 7740121-Methanesulfonylpiperidine-4-carboxylic acid수율 73%

시약·촉매·용매 3

HCID 23938Palladium촉매HCID 887Methanol용매HCID 8857Ethyl Acetate용매

실험 절차

1-Methanesulfonyl-piperidine-4-carboxylic acid benzyl ester (0.8 g, 26.7 mmol) from step 4, was dissolved in ethyl acetate (100 ml) and methanol (10 ml), Pd/C 10% (80 mg) was added and the resulting mixture was hydrogenated at 1 bar. The catalyst was filtered over celite, the solvent was removed under reduced pressure to give a white solid. Yield 73%, 0.4 g

후처리

  1. filtrationThe catalyst was filtered over celite
  2. customthe solvent was removed under reduced pressure
  3. customto give a white solid

출처 및 근거

ORD 기록
ord-225dcdbf5dfe458cac1b8eed46071949
출처 데이터셋
uspto-grants-2016_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09233115B2

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