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

HRID 574323노트

반응식

HRID 574323 반응식
C[Si]([N-][Si](C)(C)C)(C)C.[K+].[Cl:11][C:12]1[N:17]2[N:18]=[C:19]([C:21]3[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=3)[CH:20]=[C:16]2[N:15]=[C:14]([CH3:27])[C:13]=1[CH2:28][C:29]([O:31][CH3:32])=[O:30].C1(C2[O:41]N2S(C2C=CC=CC=2)(=O)=O)C=CC=CC=1>C1COCC1>[Cl:11][C:12]1[N:17]2[N:18]=[C:19]([C:21]3[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=3)[CH:20]=[C:16]2[N:15]=[C:14]([CH3:27])[C:13]=1[CH:28]([OH:41])[C:29]([O:31][CH3:32])=[O:30]

참가 물질

5

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온도
-78 °C

실험 절차

To a stirred solution of KHMDS (0.5 M in toluene, 9.50 mL, 4.75 mmol) in THF (24 mL) at −78° C. was added a solution of methyl 2-(7-chloro-5-methyl-2-phenylpyrazolo[1,5-a]pyrimidin-6-yl)acetate (1 g, 3.17 mmol) in THF (24 mL) drop wise over 40 min. The mixture was stirred at −78° C. for 30 min. A solution of 3-phenyl-2-(phenylsulfonyl)-1,2-oxaziridine (1.241 g, 4.75 mmol) in THF (24 mL) was added over 20 min and the reaction mixture was stirred for additional 30 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 (535 mg, 50.9%). 1H-NMR (500 MHz, CDCl3) δ 2.62 (3 H, s), 3.83 (3 H, s), 5.29 (1 H, s), 5.76 (1 H, s), 6.94 (1 H, s), 7.38-7.50 (3 H, m), 8.00-8.02 (2 H, m).

후처리

  1. stirringthe reaction mixture was stirred for additional 30 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

출처 및 근거

ORD 기록
ord-89a32f0499b24ab0981bbb6ddc2e114c
출처 데이터셋
uspto-grants-2015_05
특허 번호
US09034882B2

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