Sodium hydride → tert-Butyl {4-[5-(trans-2-fluorocyclohexyloxy)-7-propoxyoxazolo[5,4-d]pyrimidin-2-yl]-2,6-dimethylphenoxy}acetate

HRID 81507

反応式

HRID 81507 の反応式
[F:1][C@@H:2]1[CH2:7][CH2:6][CH2:5][CH2:4][C@H:3]1[OH:8].[H-].[Na+].CS([C:15]1[N:16]=[C:17]([O:41][CH2:42][CH2:43][CH3:44])[C:18]2[N:23]=[C:22]([C:24]3[CH:38]=[C:37]([CH3:39])[C:27]([O:28][CH2:29][C:30]([O:32][C:33]([CH3:36])([CH3:35])[CH3:34])=[O:31])=[C:26]([CH3:40])[CH:25]=3)[O:21][C:19]=2[N:20]=1)(=O)=O>CN(C)C=O>[F:1][C@@H:2]1[CH2:7][CH2:6][CH2:5][CH2:4][C@H:3]1[O:8][C:15]1[N:16]=[C:17]([O:41][CH2:42][CH2:43][CH3:44])[C:18]2[N:23]=[C:22]([C:24]3[CH:25]=[C:26]([CH3:40])[C:27]([O:28][CH2:29][C:30]([O:32][C:33]([CH3:34])([CH3:35])[CH3:36])=[O:31])=[C:37]([CH3:39])[CH:38]=3)[O:21][C:19]=2[N:20]=1

参加物

5

実験手順

Under an atmosphere of argon and at 0 C, 26 mg of trans-2-fluorocyclohexanol were added to a suspension of 10 mg of sodium hydride (60% in mineral oil) in 2 ml of N,N-dimethylformamide. After 15 min, a solution of 100 mg of tert-butyl [4-(5-methanesulfonyl-7-propoxyoxazolo[5,4-d]pyrimidin-2-yl)-2,6-dimethylphenoxy]acetate in 1 ml of N,N-dimethylformamide was slowly added. After 12 h at room temperature, the mixture was quenched by addition of water and extracted twice with ethyl acetate. The combined organic layers were dried and concentrated under reduced pressure. This gave 101 mg of the title compound.

後処理

  1. waitAfter 12 h at room temperature
  2. customthe mixture was quenched by addition of water
  3. extractionextracted twice with ethyl acetate
  4. customThe combined organic layers were dried
  5. concentrationconcentrated under reduced pressure

出典と根拠

ORDレコード
ord-b471f888480945b7ae876a55e18b2f8f
出典データセット
uspto-grants-2014_09
特許番号
US08846691B2

関連ノート

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