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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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HCID 178448823, 화합물 → HCID 178448828, 화합물

HRID 1658523
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HRID 1658523 반응식
[CH2:1]([NH:5][C:6]1[C:11]([N+:12]([O-])=O)=[C:10]([SH:15])[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]>[Zn].C(O)(=O)C>[NH2:12][C:11]1[C:6]([NH:5][CH2:1][CH2:2][CH2:3][CH3:4])=[C:7]([C:17]([O:19][CH2:20][CH3:21])=[O:18])[C:8]([CH3:16])=[N:9][C:10]=1[SH:15]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 178448823HCID 178448823, 화합물

생성물 1

HCID 178448828HCID 178448828, 화합물

시약·촉매·용매 2

HCID 23994Zinc촉매HCID 176Acetic Acid용매

실험 절차

6.2 g. of 4-butylamino-6-mercapto-2-methyl-5 -nitropyridine- 3-carboxylic acid, ethyl ester (0.02 mol.) are dissolved in 25 ml. of acetic acid at reflux temperature with stirring. Zinc dust is added cautiously in small portions until the solvent is colorless. The inorganic preceipitate is then filtered off, the solvent removed and the residue dissolved in 10 ml. of methanol. The product, 5-amino-4-butylamino-6-mercapto-2-methylpyridine-3-carboxylic acid, ethyl ester, precipitates after the addition of aqueous ammonia, yield 3.6 g. (64%); m.p. 103°-105° (ethyl acetate).

후처리

  1. filtrationThe inorganic preceipitate is then filtered off
  2. customthe solvent removed
  3. dissolutionthe residue dissolved in 10 ml
  4. customThe product, 5-amino-4-butylamino-6-mercapto-2-methylpyridine-3-carboxylic acid, ethyl ester, precipitates
  5. additionafter the addition of aqueous ammonia, yield 3.6 g

출처 및 근거

ORD 기록
ord-5deba5309fdd4ca3affaa13a7164e2e2
출처 데이터셋
uspto-grants-1976_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US03965108

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