tert-Butanol → Tert-butyl{2-[(3-chlorophenyl)amino]-4-(trifluoromethyl)pyrimidin-5-yl}carbamate

HRID 38791

反応式

HRID 38791 の反応式
[Cl:1][C:2]1[CH:3]=[C:4]([NH:8][C:9]2[N:14]=[C:13]([C:15]([F:18])([F:17])[F:16])[C:12](C(O)=O)=[CH:11][N:10]=2)[CH:5]=[CH:6][CH:7]=1.C([N:24](CC)CC)C.C1(P(N=[N+]=[N-])(C2C=CC=CC=2)=O)C=CC=CC=1.[C:46](=[O:49])([O-])[OH:47].[Na+].[C:51](O)([CH3:54])([CH3:53])[CH3:52]>>[Cl:1][C:2]1[CH:3]=[C:4]([NH:8][C:9]2[N:14]=[C:13]([C:15]([F:16])([F:17])[F:18])[C:12]([NH:24][C:46](=[O:49])[O:47][C:51]([CH3:54])([CH3:53])[CH3:52])=[CH:11][N:10]=2)[CH:5]=[CH:6][CH:7]=1

参加物

6

反応条件

温度
90 °C

実験手順

To a mixture of 2-[(3-chlorophenyl)amino]-4-(trifluoromethyl)pyrimidine-5-carboxylic acid (307 mg), triethylamine (162 μL), and tert-butyl alcohol (9 mL) was added diphenylphosphorylazide (250 μL), followed by stirring at 90° C. for 7 hours. To the reaction mixture was added a saturated aqueous sodium hydrogen carbonate solution (50 mL), followed by extraction with ethyl acetate (50 mL), and then the extract was washed with saturated brine (30 mL). The organic layer was dried over anhydrous magnesium sulfate and then concentrated under reduced pressure, and the obtained residue was purified by silica gel column chromatography (eluent: hexane-ethyl acetate) to obtain tert-butyl {2-[(3-chlorophenyl)amino]-4-(trifluoromethyl)pyrimidin-5-yl}carbamate (270 mg) as a pale yellow powder.

後処理

  1. extractionfollowed by extraction with ethyl acetate (50 mL)
  2. washthe extract was washed with saturated brine (30 mL)
  3. dry with materialThe organic layer was dried over anhydrous magnesium sulfate
  4. concentrationconcentrated under reduced pressure
  5. customthe obtained residue was purified by silica gel column chromatography (eluent: hexane-ethyl acetate)

出典と根拠

ORDレコード
ord-cc9395f6678a4328bd0405ccf8eb2dbe
出典データセット
uspto-grants-2013_09
特許番号
US08524727B2

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