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Isobutylamine → Methyl 4-[(2-methylpropyl)amino]-3-nitrobenzoate

HRID 410896
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HRID 410896 반응식
Cl[C:2]1[CH:11]=[CH:10][C:5]([C:6]([O:8][CH3:9])=[O:7])=[CH:4][C:3]=1[N+:12]([O-:14])=[O:13].[CH2:15]([NH2:19])[CH:16]([CH3:18])[CH3:17]>CN(C=O)C>[CH3:9][O:8][C:6](=[O:7])[C:5]1[CH:10]=[CH:11][C:2]([NH:19][CH2:15][CH:16]([CH3:18])[CH3:17])=[C:3]([N+:12]([O-:14])=[O:13])[CH:4]=1
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참가 물질

4

반응물 2

HCID 6558IsobutylamineHCID 735797Methyl 4-chloro-3-nitrobenzoate

생성물 1

HCID 67334709Methyl 4-[(2-methylpropyl)amino]-3-nitrobenzoate수율 81.2%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

4-Isobutylamino-3-nitro-benzoic acid methyl ester (950.0 mg) was prepared by following General Procedure A starting from methyl 4-chloro-3-nitrobenzoate (1.0 g) and isobutyl amine (402.0 mg) in DMF (10.0 mL). The crude product was used in the next step without further purification.

후처리

  1. customThe crude product was used in the next step without further purification

출처 및 근거

ORD 기록
ord-78d043cda1874fedb620d3037bde705b
출처 데이터셋
uspto-grants-2014_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08759535B2

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