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Ammonia → 6-Amino-4-butylamino-2-methyl-5-nitronicotinic acid ethyl ester

HRID 1287232
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반응식

HRID 1287232 반응식
[CH2:1]([NH:5][C:6]1[C:11]([N+:12]([O-:14])=[O:13])=[C:10](Cl)[N:9]=[C:8]([CH3:16])[C:7]=1[C:17]([O:19][CH2:20][CH3:21])=[O:18])[CH2:2][CH2:3][CH3:4].[NH3:22]>CO>[NH2:22][C:10]1[N:9]=[C:8]([CH3:16])[C:7]([C:17]([O:19][CH2:20][CH3:21])=[O:18])=[C:6]([NH:5][CH2:1][CH2:2][CH2:3][CH3:4])[C:11]=1[N+:12]([O-:14])=[O:13]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 222AmmoniaHCID 123875984-Butylamino-6-chloro-2-methyl-5-nitronicotinic acid ethyl ester

생성물 1

HCID 123876046-Amino-4-butylamino-2-methyl-5-nitronicotinic acid ethyl ester

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

177.9 g. of 4-butylamino-6-chloro-2-methyl-5-nitropyridine-3-carboxylic acid, ethyl ester (0.5 Mol.) dissolved in 500 ml. of methanol are heated with 300 ml. of aqueous ammonia (30%) in an autoclave at about 60° for 10 hours. After this time, the solvent is distilled off and the residual 6-amino-4-butylamino-2-methyl-5-nitropyridine-3-carboxylic acid, ethyl ester is recrystallized from methanol, yield 135 g.; m.p. 98°-99°.

후처리

  1. distillationAfter this time, the solvent is distilled off
  2. customthe residual 6-amino-4-butylamino-2-methyl-5-nitropyridine-3-carboxylic acid, ethyl ester is recrystallized from methanol, yield 135 g

출처 및 근거

ORD 기록
ord-0716dd700925473e8c7605f66456f495
출처 데이터셋
uspto-grants-1976_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US03984412

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