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HCID 57659246、化合物 → (RS)-S-(3-aminophenyl)-N-(isopropylcarbamoyl)-S-methylsulfoximide

HRID 238140
ノート
印刷プレビュー

反応式

HRID 238140 の反応式
[N+:1]([C:4]1[CH:5]=[C:6]([S:10]([CH3:19])(=[N:12][C:13](=[O:18])[NH:14][CH:15]([CH3:17])[CH3:16])=[O:11])[CH:7]=[CH:8][CH:9]=1)([O-])=O>C(O)C.Cl.CO.[Fe]>[NH2:1][C:4]1[CH:5]=[C:6]([S:10]([CH3:19])(=[N:12][C:13](=[O:18])[NH:14][CH:15]([CH3:16])[CH3:17])=[O:11])[CH:7]=[CH:8][CH:9]=1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

6

反応物 1

HCID 57659246HCID 57659246、化合物

生成物 1

HCID 57659241(RS)-S-(3-aminophenyl)-N-(isopropylcarbamoyl)-S-methylsulfoximide収率 65%

試薬・触媒・溶媒 4

HCID 23925Iron触媒HCID 313Hydrochloric Acid溶媒HCID 702Ethanol溶媒HCID 887Methanol溶媒

反応条件

温度
60 °C

実験手順

18.61 g iron powder in 198 ml ethanol and 1.93 ml conc. hydrochloric acid were stirred for 30 minutes at room temperature. 7.8 g (27.34 mmol) (RS)—S-(3-nitrophenyl)-N-(isopropylcarbamoyl)-S-methylsulfoximide in 20 ml methanol were added. The mixture was stirred at 60° C. for 2 hours and filtered over a bed of silica gel. The residue was washed with hot ethanol. The combined filtrates were evaporated. The crude residue was purified by column chromatography (silica gel, dichloromethane:dichloromethane/ethanol 1:1) to give 4.53 g (65% yield) of the title compound.

後処理

  1. filtrationfiltered over a bed of silica gel
  2. washThe residue was washed with hot ethanol
  3. customThe combined filtrates were evaporated
  4. customThe crude residue was purified by column chromatography (silica gel, dichloromethane:dichloromethane/ethanol 1:1)

出典と根拠

ORDレコード
ord-4986fd5c74984702b073bd8e6d641ecb
出典データセット
uspto-grants-2014_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08642611B2

反応ノート

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