2-(Benzenesulfonyl)-3-phenyloxaziridine → Methyl 2-(2-bromo-7-chloro-5-methylpyrazolo[1,5-a]pyrimidin-6-yl)-2-hydroxyacetate

HRID 574340ノート

反応式

HRID 574340 の反応式
C[Si]([N-][Si](C)(C)C)(C)C.[K+].[Br:11][C:12]1[CH:27]=[C:15]2[N:16]=[C:17]([CH3:26])[C:18]([CH2:21][C:22]([O:24][CH3:25])=[O:23])=[C:19]([Cl:20])[N:14]2[N:13]=1.C1(C2[O:36]N2S(C2C=CC=CC=2)(=O)=O)C=CC=CC=1>C1COCC1>[Br:11][C:12]1[CH:27]=[C:15]2[N:16]=[C:17]([CH3:26])[C:18]([CH:21]([OH:36])[C:22]([O:24][CH3:25])=[O:23])=[C:19]([Cl:20])[N:14]2[N:13]=1

参加物

5

反応条件

温度
-78 °C

実験手順

To a stirred solution of KHMDS (0.5 M in toluene, 2.83 mL, 1.413 mmol) in THF (6 mL) at −78° C. was added a solution of methyl 2-(2-bromo-7-chloro-5-methylpyrazolo[1,5-a]pyrimidin-6-yl)acetate (300 mg, 0.942 mmol) in THF (6 mL) dropwise over 20 min. The mixture was stirred at −78° C. for 30 min. A solution of 3-phenyl-2-(phenylsulfonyl)-1,2-oxaziridine (369 mg, 1.413 mmol) in THF (6 mL) was added over 15 min and the reaction mixture was stirred for additional 60 min at −78° C. The reaction mixture was quenched with saturated NH4Cl aqueous solution (4 mL). The reaction mixture was allowed to warm to room temperature and then diluted with ethyl acetate (100 mL). The organic phase was washed with water and brine and dried with sodium sulfate. The solvent was evaporated. Purification by silica gel chromatography provided the title compound (85 mg, 27%). 1H NMR (400 MHz, CHLOROFORM-d) δ 2.63 (3 H, s), 3.84 (3 H, s), 5.74 (1 H, s), 6.71 (1 H, s).

後処理

  1. stirringthe reaction mixture was stirred for additional 60 min at −78° C
  2. customThe reaction mixture was quenched with saturated NH4Cl aqueous solution (4 mL)
  3. temperatureto warm to room temperature
  4. additiondiluted with ethyl acetate (100 mL)
  5. washThe organic phase was washed with water and brine
  6. dry with materialdried with sodium sulfate
  7. customThe solvent was evaporated
  8. customPurification by silica gel chromatography

出典と根拠

ORDレコード
ord-656c98dca39a41a5ba5ac64edd34d468
出典データセット
uspto-grants-2015_05
特許番号
US09034882B2

反応ノート

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