Trisodium Phosphate → Isotorabine

HRID 19491

反応式

HRID 19491 の反応式
[NH2:1][C:2]1[N:3]=[CH:4][C:5]2[S:10][C:9](=[O:11])[N:8]([C@@H:12]3[O:24][C@H:23]([CH2:25][O:26]C(=O)C)[C@@H:18]([O:19][C:20](=[O:22])[CH3:21])[C@H:13]3[O:14][C:15](=[O:17])[CH3:16])[C:6]=2[N:7]=1.P([O-])([O-])([O-])=O.[Na+].[Na+].[Na+]>CC(C)=O>[NH2:1][C:2]1[N:3]=[CH:4][C:5]2[S:10][C:9](=[O:11])[N:8]([C@@H:12]3[O:24][C@H:23]([CH2:25][OH:26])[C@@H:18]([O:19][C:20](=[O:22])[CH3:21])[C@H:13]3[O:14][C:15](=[O:17])[CH3:16])[C:6]=2[N:7]=1

参加物

4

実験手順

To a clear solution of 78 (500 mg) in acetone (5 mL) was added sodium phosphate buffer (pH=7.0, 0.1 M, 25 mL), upon which the solution became cloudy (white precipitate). Candida antarctica lipase resin (250 mg) was added to the mixture and the suspension was subsequently gently shaken for 10 h at room temperature. The resulting clear mixture was filtered, and organic solvent was removed under vacuum. The aqueous solution was then extracted with ethyl acetate (3×25 mL) and the organic layers were combined, dried over MgSO4, and concentrated. The resulting solid could be further purified in a manner similar to that described in Example 43, step 3.

後処理

  1. filtrationThe resulting clear mixture was filtered
  2. customorganic solvent was removed under vacuum
  3. extractionThe aqueous solution was then extracted with ethyl acetate (3×25 mL)
  4. dry with materialdried over MgSO4
  5. concentrationconcentrated
  6. customThe resulting solid could be further purified in a manner similar to

出典と根拠

ORDレコード
ord-8553f3f407f5462680d176d3a9b20f55
出典データセット
uspto-grants-2010_06
特許番号
US07745415B2

関連ノート

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