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Ethylene Oxide → 2-Sulfamoyl-6-(2-hydroxyethyl)-4,5,6,7-tetrahydrothieno[2,3-c]pyridine

HRID 569051
ノート
印刷プレビュー

反応式

HRID 569051 の反応式
[S:1]([C:5]1[S:13][C:8]2[CH2:9][NH:10][CH2:11][CH2:12][C:7]=2[CH:6]=1)(=[O:4])(=[O:3])[NH2:2].[CH2:14]1[O:16][CH2:15]1>CO.C(#N)C>[S:1]([C:5]1[S:13][C:8]2[CH2:9][N:10]([CH2:14][CH2:15][OH:16])[CH2:11][CH2:12][C:7]=2[CH:6]=1)(=[O:3])(=[O:4])[NH2:2]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 2

HCID 6354Ethylene OxideHCID 201485892-Sulfamoyl-4,5,6,7-tetrahydrothieno[2,3-c]pyridine

生成物 1

HCID 201485792-Sulfamoyl-6-(2-hydroxyethyl)-4,5,6,7-tetrahydrothieno[2,3-c]pyridine収率 80%

試薬・触媒・溶媒 2

HCID 887Methanol溶媒HCID 6342Acetonitrile溶媒

実験手順

Into a solution of 2-sulfamoyl-4,5,6,7-tetrahydrothieno[2,3-c]pyridine (1.74 g, 8.0 mmol) in methanol (25 ml) and acetonitrile (50 ml) was bubbled ethylene oxide gas for 10 minutes. The reaction vessel was stoppered and the mixture was stirred for 18 hours. The precipitated product was collected by filtration. The filtrates were concentrated to provide additional product (total weight, 2.02 g). This material was crystallized from acetonitrile to give 1.67 g (80% yield) of pure product; m.p. 184°-186° C.

このページの内容参加物実験手順後処理出典と根拠反応ノート

後処理

  1. filtrationThe precipitated product was collected by filtration
  2. concentrationThe filtrates were concentrated
  3. customto provide additional product (total weight, 2.02 g)
  4. customThis material was crystallized from acetonitrile

出典と根拠

ORDレコード
ord-66ed44e2459c46779b3a0b1a8964cfca
出典データセット
uspto-grants-1988_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04731368

反応ノート

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