Water → HCID 23368712、化合物

HRID 1901808ノート

反応式

HRID 1901808 の反応式
[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([NH:17][S:18]([C:21]2[CH:27]=[CH:26][C:24]([CH3:25])=[CH:23][CH:22]=2)(=[O:20])=[O:19])=[C:6]([CH:16]=1)[C:7]([C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][C:10]=1[Cl:15])=[O:8].[H-].[Na+].[CH3:30]C(C)(Br)C(N)=O.O.[CH3:38][N:39]([CH:41]=[O:42])[CH3:40]>>[S:18]([N:17]([C:5]1[CH:4]=[CH:3][C:2]([Cl:1])=[CH:16][C:6]=1[C:7]([C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][C:10]=1[Cl:15])=[O:8])[CH2:30][C:41](=[O:42])[N:39]([CH3:40])[CH3:38])([C:21]1[CH:22]=[CH:23][C:24]([CH3:25])=[CH:26][CH:27]=1)(=[O:19])=[O:20]

参加物

6

実験手順

8.4 g of 5,2'-dichloro-2-tosylaminobenzophenone are dissolved in 40 ml of DMF and treated with 0.7 g of 80% sodium hydride; after 15 minutes, 10 g of dimethylbromoacetamide, prepared in Example 1, are added and the mixture is stirred overnight at RT. The reaction medium is poured into water, the precipitate formed is filtered off and taken up with DCM and the solution is dried and concentrated. 9.2 g of the expected product are obtained after crystallization from isopropyl ether.

後処理

  1. additionare added
  2. customthe precipitate formed
  3. filtrationis filtered off
  4. customthe solution is dried
  5. concentrationconcentrated

出典と根拠

ORDレコード
ord-29acb750a2bd4746abf09d8eb740e933
出典データセット
uspto-grants-1996_11
特許番号
US05578633

反応ノート

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