Hydrochloric Acid → 3-(Pyridin-3-yl)-4-phenyl-1,2,5-thiadiazole-1,1-dioxide Hydrochloride

HRID 2053629ノート

反応式

HRID 2053629 の反応式
[ClH:1].[C:2]1([C:8](=O)[C:9]([C:11]2[CH:12]=[N:13][CH:14]=[CH:15][CH:16]=2)=O)[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[S:18]([NH2:22])([NH2:21])(=[O:20])=[O:19]>CO>[ClH:1].[N:13]1[CH:14]=[CH:15][CH:16]=[C:11]([C:9]2[C:8]([C:2]3[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=3)=[N:22][S:18](=[O:20])(=[O:19])[N:21]=2)[CH:12]=1

参加物

5

反応物 3

HCID 313Hydrochloric AcidHCID 82267SulfamideHCID 109875561-Phenyl-2-(pyridin-3-yl)ethan-1,2-dione

生成物 1

HCID 685697783-(Pyridin-3-yl)-4-phenyl-1,2,5-thiadiazole-1,1-dioxide Hydrochloride

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

反応条件

温度
65 °C

実験手順

Hydrogen chloride gas is bubbled into a solution of 1-phenyl-2-(pyridin-3-yl)ethan-1,2-dione (1.63 g, 7.7 mmol, J. Org. Chem., 1999, 64, 6102) and sulfamide (750 mg, 7.7 mmol) in methanol (10 mL) until the solution begins to reflux. The gas flow is turned off, and the solution stirred at 65° C. for 3 h then cooled to rt. The solid that formed is filtered and dried to give 2.06 g of the product 497. MS: m/z 272 (M++1).

後処理

  1. temperatureto reflux
  2. temperaturethen cooled to rt
  3. customThe solid that formed
  4. filtrationis filtered
  5. customdried

出典と根拠

ORDレコード
ord-865c7bf6da804114910cc1932dd4b093
出典データセット
uspto-grants-2008_02
特許番号
US07326792B2

反応ノート

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