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Thiosemicarbazide Hydrochloride → HCID 178491699, 화합물

HRID 1089983
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인쇄 미리보기

반응식

HRID 1089983 반응식
C(O[C:4]1[CH2:8][CH:7]([S:9][CH2:10][C:11]2[CH:16]=[CH:15][C:14]([O:17][CH3:18])=[CH:13][CH:12]=2)[CH2:6][N:5]=1)C.Cl.[NH2:20][NH:21][C:22]([NH2:24])=[S:23]>C(O)C>[CH3:18][O:17][C:14]1[CH:15]=[CH:16][C:11]([CH2:10][S:9][CH:7]2[CH2:6][NH:5][C:4](=[N:20][NH:21][C:22]([NH2:24])=[S:23])[CH2:8]2)=[CH:12][CH:13]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 3037943Thiosemicarbazide HydrochlorideHCID 104680652-Ethoxy-4-p-methoxybenzylthio-1-pyroline

생성물 1

HCID 178491699HCID 178491699, 화합물수율 21.8%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

A solution of 2-ethoxy-4-p-methoxybenzylthio-1-pyrroline (900 mg) and thiosemicarbazide hydrochloride (433 mg) in ethanol (30 ml) was refluxed under heating for 1.5 hours. The reaction solution was evaporated to dryness under reduced pressure, then the residue was distributed between ethyl acetate and 5% aqueous solution of sodium hydroxide and the organic phase was dried over Na2SO4 before the solvent was distilled off under reduced pressure. The resultant residue was passed through a column packed with 25 g of silica gel and eluted with ethyl acetate and thus 230 mg of the objective compound was obtained as colorless foam.

후처리

  1. temperatureunder heating for 1.5 hours
  2. customThe reaction solution was evaporated to dryness under reduced pressure
  3. dry with materialthe organic phase was dried over Na2SO4 before the solvent
  4. distillationwas distilled off under reduced pressure
  5. washeluted with ethyl acetate

출처 및 근거

ORD 기록
ord-2989a10ea17346a48096364ba1fbac48
출처 데이터셋
uspto-grants-1992_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05079357

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