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Water → N'-Methyl-2-(2-methyl-2-(phenylcarbonothioyl)hydrazinyl)-2-oxo-N'-(phenylcarbonothioyl)ethanesulfonohydrazide

HRID 1913511
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HRID 1913511 반응식
[CH3:1][N:2]([C:4](=[S:11])[C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][CH:6]=1)[NH2:3].Cl[S:13]([CH2:16][C:17](Cl)=[O:18])(=[O:15])=[O:14].O>C(Cl)Cl.N1C=CC=CC=1>[CH3:1][N:2]([C:4]([C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][CH:6]=1)=[S:11])[NH:3][S:13]([CH2:16][C:17]([NH:3][N:2]([CH3:1])[C:4]([C:5]1[CH:6]=[CH:7][CH:8]=[CH:9][CH:10]=1)=[S:11])=[O:18])(=[O:15])=[O:14]
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참가 물질

6

반응물 3

HCID 962WaterHCID 77642(Chlorosulphonyl)acetyl chlorideHCID 12206211N-methylbenzothiohydrazide

생성물 1

HCID 59267374N'-Methyl-2-(2-methyl-2-(phenylcarbonothioyl)hydrazinyl)-2-oxo-N'-(phenylcarbonothioyl)ethanesulfonohydrazide수율 36.6%

시약·촉매·용매 2

HCID 1049Pyridine용매
HCID 6344
Dichloromethane
용매

실험 절차

To a 0° C. solution of N-methylbenzothiohydrazide (10 mmol) in DCM (20 mL) and pyridine (1 mL) was added 2-(chlorosulfonyl)acetyl chloride (5 mmol) dropwise. The mixture was kept at rt for 2 h before it was poured into water (20 ml). The organic layer was separated, dried and evaporated and the resulting residue was purified by column chromatography to give compound 68 as yellowish solids (0.8 g). 1H-NMR (CDCl3) δ 10.5 (m, 1H), 7.4 (m, 10H), 4.4 (m, 1H), 3.4-3.8 (m, 8H) ppm; ESMS calcd for C18H20N4O3S3:436.1; found: 437.2 (M+H+).

후처리

  1. customThe organic layer was separated
  2. customdried
  3. customevaporated
  4. customthe resulting residue was purified by column chromatography

출처 및 근거

ORD 기록
ord-c7727f6a340942459d6d02d38eb31441
출처 데이터셋
uspto-grants-2013_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08609720B2

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