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Water → 2-(2-Acetylhydrazino)-5-(2-methylphenyl)-1,3,4-thiadiazole

HRID 25957
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HRID 25957 반응식
Cl.[NH:2]([C:4]1[S:5][C:6]([C:9]2[CH:14]=[CH:13][CH:12]=[CH:11][C:10]=2[CH3:15])=[N:7][N:8]=1)[NH2:3].O.[C:17](OC(=O)C)(=[O:19])[CH3:18]>N1C=CC=CC=1>[C:17]([NH:3][NH:2][C:4]1[S:5][C:6]([C:9]2[CH:14]=[CH:13][CH:12]=[CH:11][C:10]=2[CH3:15])=[N:7][N:8]=1)(=[O:19])[CH3:18]
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참가 물질

5

반응물 3

HCID 962WaterHCID 7918Acetic AnhydrideHCID 30501311,3,4-Thiadiazol-2(3H)-one, 5-(2-methylphenyl)-, hydrazone, monohydrochloride

생성물 1

HCID 136840272-(2-Acetylhydrazino)-5-(2-methylphenyl)-1,3,4-thiadiazole

시약·촉매·용매 1

HCID 1049Pyridine용매

실험 절차

A solution of 2-hydrazino-5-(2-methylphenyl)-1,3,4-thiadiazole hydrochloride (1.0 g) in a mixture of acetic anhydride (0.5 ml) and pyridine (0.5 ml) was kept at room temperature under nitrogen for 0.5 hr. The solution was poured into water (100 ml) and extracted three times with methylene chloride. The organic layer was evaporated and the residue was fractionated on two 20 × 20 cm, 2 mm thick silica preparative t.l.c. plates by eluting with chloroform-methanol (4:1). The resultant product was crystallised from ethyl acetate (0.32 g; 31%) m.p. 165°-6°. C11H12N4OS requires C, 52.8; H, 5.6; N, 22.4; S, 12.8 Found C, 52.8; H, 5.1; N, 22.8; S, 13.2%

후처리

  1. extractionextracted three times with methylene chloride
  2. customThe organic layer was evaporated
  3. washplates by eluting with chloroform-methanol (4:1)
  4. customThe resultant product was crystallised from ethyl acetate (0.32 g; 31%) m.p. 165°-6°

출처 및 근거

ORD 기록
ord-2c5a6dd7d1a84bc39915fb88606761fb
출처 데이터셋
uspto-grants-1979_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04147794

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