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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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HCID 178469258, 화합물 → HCID 178469256, 화합물

HRID 1658524
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HRID 1658524 반응식
[CH: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])([CH2:3][CH3:4])[CH3:2]>[Fe].C(O)(=O)C>[NH2:12][C:11]1[C:6]([NH:5][CH:1]([CH2:3][CH3:4])[CH3:2])=[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 178469258HCID 178469258, 화합물

생성물 1

HCID 178469256HCID 178469256, 화합물

시약·촉매·용매 2

HCID 23925Iron촉매HCID 176Acetic Acid용매

실험 절차

6.2 g. of 4-sec.butylamino-6-mercapto-2-methyl-5-nitropyridine-3-carboxylic acid, ethyl ester are dissolved in 50 ml. of acetic acid. Iron dust is added carefully at reflux temperature until the mixture is colorless. The excess of iron is filtered off and the filtrate is evaporated to dryness. The oily residue is dissolved in 10 ml. of methanol and precipitated by the addition of aqueous ammonia to obtain 5-amino-4-sec.butylamino-6-mercapto-2-methylpyridine-3-carboxylic acid, ethyl ester, yield 3 g. (53%); m.p. 88°-89° (ethyl acetate).

후처리

  1. temperatureat reflux temperature until the mixture
  2. filtrationThe excess of iron is filtered off
  3. customthe filtrate is evaporated to dryness
  4. dissolutionThe oily residue is dissolved in 10 ml
  5. customof methanol and precipitated by the addition of aqueous ammonia

출처 및 근거

ORD 기록
ord-5b50792b90814ca795934a83d214c8ce
출처 데이터셋
uspto-grants-1976_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US03965108

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