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Methanol → Methyl 3-amino-5-[methyl(methylsulfonyl)amino]benzoate

HRID 1160449
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인쇄 미리보기

반응식

HRID 1160449 반응식
[CH3:1][N:2]([S:16]([CH3:19])(=[O:18])=[O:17])[C:3]1[CH:4]=[C:5]([CH:10]=[C:11]([N+:13]([O-])=O)[CH:12]=1)[C:6]([O:8][CH3:9])=[O:7].CO>[Pd].C(OCC)(=O)C>[NH2:13][C:11]1[CH:10]=[C:5]([CH:4]=[C:3]([N:2]([CH3:1])[S:16]([CH3:19])(=[O:18])=[O:17])[CH:12]=1)[C:6]([O:8][CH3:9])=[O:7]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 887MethanolHCID 57815130Methyl 3-[(methanesulfonyl)(methyl)amino]-5-nitrobenzoate

생성물 1

HCID 21054739Methyl 3-amino-5-[methyl(methylsulfonyl)amino]benzoate수율 99%

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 8857Ethyl Acetate용매

실험 절차

A mixture of methyl 3-[methyl(methylsulfonyl)amino]-5-nitrobenzoate obtained in Reference Example 95.76 g (20 mmol), 10% Pd/C (50% wet) (1.50 g), methanol (80 mL) and ethyl acetate (80 mL) was stirred at room temperature under hydrogen atmosphere for 1.5 hours. The reaction solution was filtered on Celite and the solvent was evaporated to give 5.11 g (19.8 mmol) of the title compound (yield: 99%).

후처리

  1. filtrationThe reaction solution was filtered on Celite
  2. customthe solvent was evaporated

출처 및 근거

ORD 기록
ord-6d79eb5f11344096a452566a6dec06c5
출처 데이터셋
uspto-grants-2010_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07816387B2

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