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Hydrazine hydrate (1:1) → HCID 12813042, 화합물

HRID 1902465
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HRID 1902465 반응식
[CH3:1][O:2][C:3]1[CH:4]=[C:5]([C:13]2[S:14][C:15]([C:19]([O:21]CC)=O)=[C:16]([CH3:18])[N:17]=2)[CH:6]=[C:7]([O:11][CH3:12])[C:8]=1[O:9][CH3:10].O.[NH2:25][NH2:26]>C(O)C>[CH3:1][O:2][C:3]1[CH:4]=[C:5]([C:13]2[S:14][C:15]([C:19]([NH:25][NH2:26])=[O:21])=[C:16]([CH3:18])[N:17]=2)[CH:6]=[C:7]([O:11][CH3:12])[C:8]=1[O:9][CH3:10]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 24654Hydrazine hydrate (1:1)HCID 12813041HCID 12813041, 화합물

생성물 1

HCID 12813042HCID 12813042, 화합물수율 59%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

Ethyl 2-(3,4,5-trimethoxyphenyl)-4-methylthiazole-5-carboxylate prepared in Example 4 (6.2 g corresponding to its 0.02 mol), 6.1 g (0.1 mol) of hydrazine hydrate of purity of 82% and 150 ml of ethanol were heated for 6 hours at a temperature of 90° C. The crystals, which separated out after cooling the reaction mixture, were recrystallized from 95% aqueous ethanolic solution to obtain the object consisting of faintly yellow scale-like crystals, amounting to 3.8 g and melting at 179.5° to 181° C. at a yield of 59%.

후처리

  1. customThe crystals, which separated out
  2. temperatureafter cooling the reaction mixture
  3. customwere recrystallized from 95% aqueous ethanolic solution
  4. customto obtain the object

출처 및 근거

ORD 기록
ord-51919f7835404f2d84910756b0c3583f
출처 데이터셋
uspto-grants-1982_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04363813

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