Thiophene-3-sulfonyl Chloride → HCID 12146375、化合物

HRID 232748

反応式

HRID 232748 の反応式
[S:1]1[CH:5]=[CH:4][C:3]([S:6](Cl)(=[O:8])=[O:7])=[CH:2]1.[NH2:10][C:11]1[O:15][N:14]=[C:13]([CH3:16])[C:12]=1[Br:17]>>[Br:17][C:12]1[C:13]([CH3:16])=[N:14][O:15][C:11]=1[NH:10][S:6]([C:3]1[CH:4]=[CH:5][S:1][CH:2]=1)(=[O:8])=[O:7]

参加物

3

反応物 2

HCID 2776378Thiophene-3-sulfonyl ChlorideHCID 104875194-Bromo-3-methylisoxazol-5-amine

生成物 1

HCID 12146375HCID 12146375、化合物収率 22%

実験手順

N-(4-Bromo-3-methyl-5-isoxazolyl)thiophene-3-sulfonamide was prepared in the same manner as described in Example 2 from thiophene-3-sulfonyl chloride with 5-amino-4-bromo-3-methylisoxazole in 22% yield. Purification by column chromatography using 10% MeOH/CHCl3 as eluent gave a pale brown oil.

後処理

  1. customPurification by column chromatography
  2. customgave a pale brown oil

出典と根拠

ORDレコード
ord-5648f23a8a5649a0a6503bd53864150c
出典データセット
uspto-grants-1997_01
特許番号
US05591761

関連ノート

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