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

HRID 1913511
ノート
印刷プレビュー

反応式

HRID 1913511 の反応式
[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]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 3

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

生成物 1

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

試薬・触媒・溶媒 2

HCID 1049Pyridine溶媒
HCID 6344
Dichloromethane
溶媒

実験手順

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+).

後処理

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

出典と根拠

ORDレコード
ord-c7727f6a340942459d6d02d38eb31441
出典データセット
uspto-grants-2013_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08609720B2

反応ノート

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