Trichloromethanesulfenyl chloride → 5-Chloro-3-(propan-2-yl)-1,2,4-thiadiazole

HRID 1496648

反応式

HRID 1496648 の反応式
Cl.[CH3:2][CH:3]([CH3:7])[C:4](=[NH:6])[NH2:5].[Cl:8][C:9](Cl)(Cl)[S:10]Cl.[OH-].[Na+]>C(Cl)Cl>[Cl:8][C:9]1[S:10][N:5]=[C:4]([CH:3]([CH3:7])[CH3:2])[N:6]=1

参加物

5

反応条件

温度
0 °C

実験手順

To a mixture of 2-methyl propanimidamide hydrochloride (5.0 g, 40.8 mmol), trichloromethanesulfenyl chloride (7.14 g, 38.4 mmol) in methylene chloride (200 mL) at 0° C. was added dropwise an aqueous solution of sodium hydroxide (50%, 9.9 mL) over 20 minutes. The reaction mixture was stirred for 2 h at 0° C. and then was allowed to warm to room temperature, and stirred for an additional 3 h. Ice was added to the reaction mixture, the mixture was separated, and the aqueous layer was extracted with methylene chloride (3×25 mL). The combined organic extracts were dried over magnesium sulfate, filtered and concentrated under reduced pressure. The resulting residue was purified by medium pressure liquid chromatography (0 to 100% gradient of ethyl acetate in hexanes as eluant) to provide the title compound as a oil (3.8 g).

後処理

  1. temperatureto warm to room temperature
  2. stirringstirred for an additional 3 h
  3. additionIce was added to the reaction mixture
  4. customthe mixture was separated
  5. extractionthe aqueous layer was extracted with methylene chloride (3×25 mL)
  6. dry with materialThe combined organic extracts were dried over magnesium sulfate
  7. filtrationfiltered
  8. concentrationconcentrated under reduced pressure
  9. customThe resulting residue was purified by medium pressure liquid chromatography (0 to 100% gradient of ethyl acetate in hexanes as eluant)

出典と根拠

ORDレコード
ord-048a0a6735ef47c49bb88bde261263f8
出典データセット
uspto-grants-2015_12
特許番号
US09198433B2

関連ノート

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