Trichloromethanethiol → 3-Benzyl-5-chloro-1,2,4-thiadiazole

HRID 2063668

反応式

HRID 2063668 の反応式
Cl.[C:2]1([CH2:8][C:9]([NH2:11])=[NH:10])[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[Cl:12][C:13]([SH:16])(Cl)Cl.[OH-].[Na+]>ClCCl.O>[CH2:8]([C:9]1[N:11]=[C:13]([Cl:12])[S:16][N:10]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1

参加物

6

反応条件

温度
-10 °C

実験手順

To a suspension of 2-phenyl-acetamidine hydrochloride (1.078 g, 6 mmol) in dichloromethane (10 ml) was added perchloromethyl mercaptan (0.61 ml, 5 mmol) via syringe. The mixture was cooled in an ice-methanol bath to −10° C. and a solution of sodium hydroxide (1.2 g, 30 mmol) in water (3 ml) was added dropwise keeping the temperature below −8° C. After complete addition the mixture was stirred 10 min at 0° C. The reaction mixture was diluted with water and the aqueous phase was extracted three times with dichloromethane. The combined organic phases were dried over Na2SO4, filtered and the solvents were evaporated. The residue was purified by chromatography on silica gel using heptane/ethyl acetate as eluent. The title compound was obtained as an orange liquid (0.779 g, 62%). MS ISP (m/e): 211.0 (100) [(M+H)+].

後処理

  1. customthe temperature below −8° C
  2. additionAfter complete addition the mixture
  3. extractionthe aqueous phase was extracted three times with dichloromethane
  4. dry with materialThe combined organic phases were dried over Na2SO4
  5. filtrationfiltered
  6. customthe solvents were evaporated
  7. customThe residue was purified by chromatography on silica gel

出典と根拠

ORDレコード
ord-6a1148a8413e4bdcaaa3569775836b6b
出典データセット
uspto-grants-2012_10
特許番号
US08288403B2

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