홈MCP워크벤치Skills
홈워크벤치알림마이페이지
llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
  1. 홈
  2. /반응

4-Butylamino-6-chloro-2-methyl-5-nitronicotinic acid ethyl ester → HCID 178448823, 화합물

HRID 1606537
노트
인쇄 미리보기

반응식

HRID 1606537 반응식
[CH2:1]([O:3][C:4]([C:6]1[C:7]([CH3:21])=[N:8][C:9](Cl)=[C:10]([N+:17]([O-:19])=[O:18])[C:11]=1[NH:12][CH2:13][CH2:14][CH2:15][CH3:16])=[O:5])[CH3:2].O.[S-2:23].[Na+].[Na+]>O>[CH2:13]([NH:12][C:11]1[C:10]([N+:17]([O-:19])=[O:18])=[C:9]([SH:23])[N:8]=[C:7]([CH3:21])[C:6]=1[C:4]([O:3][CH2:1][CH3:2])=[O:5])[CH2:14][CH2:15][CH3:16]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 123875984-Butylamino-6-chloro-2-methyl-5-nitronicotinic acid ethyl esterHCID 19906495Sodium sulfide monohydrate

생성물 1

HCID 178448823HCID 178448823, 화합물

시약·촉매·용매 1

HCID 962Water용매

실험 절차

31.5 g. of 4-butylamino-6-chloro-2-methyl-5-nitropyridine-3-carboxylic acid ethyl ester (0.1 Mol.) are dissolved in 100 ml. of alcohol. 14.8 g. of sodium sulfide monohydrate and about 2 ml. of water are added and the mixture is stirred for one hour without cooling. The precipitated 4-butylamino-6-mercapto-2-methyl-5-nitropyridine-3-carboxylic acid, ethyl ester is filtered off, yield 27.5 g. (88%), m.p. 140°-142° (ethanol).

후처리

  1. temperaturewithout cooling
  2. filtrationThe precipitated 4-butylamino-6-mercapto-2-methyl-5-nitropyridine-3-carboxylic acid, ethyl ester is filtered off

출처 및 근거

ORD 기록
ord-7c80a20332fd47da867596a1aa962b71
출처 데이터셋
uspto-grants-1976_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US03953461

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트