Sodium Acetate → HCID 13712495、化合物

HRID 2352226ノート

反応式

HRID 2352226 の反応式
[OH:1][C:2]1[CH:15]=[C:14]2[C:5]([N:6]([C:16]([O:18][CH:19](Cl)[CH3:20])=[O:17])[C:7]3[C:12]([S:13]2)=[CH:11][CH:10]=[CH:9][CH:8]=3)=[C:4]2[CH:22]=[CH:23][CH:24]=[CH:25][C:3]=12.[C:26]([O-:29])(=[O:28])[CH3:27].[Na+]>C(O)(=O)C.C(OCC)(=O)C>[OH:1][C:2]1[CH:15]=[C:14]2[C:5]([N:6]([C:16]([O:18][CH:19]([O:29][C:26](=[O:28])[CH3:27])[CH3:20])=[O:17])[C:7]3[C:12]([S:13]2)=[CH:11][CH:10]=[CH:9][CH:8]=3)=[C:4]2[CH:22]=[CH:23][CH:24]=[CH:25][C:3]=12

参加物

5

実験手順

The product from Step 2 (4 g) and sodium acetate (6 g) were refluxed together in glacial acetic acid (60 ml) for 1 hour. The mixture was cooled, diluted with ethyl acetate (300 ml) and washed with water (3×100 ml), then with aqueous sodium bicarbonate and again with water, dried and evaporated down. The residue was chromatographed on a column of silica gel eluting with a 1:9 mixture of ethyl acetate-hexane to afford, after trituration in ether and filtration, the pure title compound (1.2 g), m.p. 195°-196° C.

後処理

  1. temperatureThe mixture was cooled
  2. washwashed with water (3×100 ml)
  3. dry with materialwith aqueous sodium bicarbonate and again with water, dried
  4. customevaporated down
  5. customThe residue was chromatographed on a column of silica gel eluting with a 1:9 mixture of ethyl acetate-hexane
  6. customto afford
  7. filtrationafter trituration in ether and filtration

出典と根拠

ORDレコード
ord-1b55da06d64d4b5ca0204eced3aacef2
出典データセット
uspto-grants-1989_10
特許番号
US04876246

反応ノート

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