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

HRID 472826
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HRID 472826 반응식
C[Si]([N-][Si](C)(C)C)(C)C.[K+].[Cl:11][C:12]1[N:17]2[N:18]=[CH:19][C:20]([C:21]3[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=3)=[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]=[CH:19][C:20]([C:21]3[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=3)=[C:16]2[N:15]=[C:14]([CH3:27])[C:13]=1[CH:28]([OH:41])[C:29]([O:31][CH3:32])=[O:30]
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참가 물질

5

반응물 3

HCID 3204052-(Benzenesulfonyl)-3-phenyloxaziridineHCID 3251421Potassium bis(trimethylsilyl)amideHCID 86670268Methyl 2-(7-chloro-5-methyl-3-phenylpyrazolo[1,5-a]pyrimidin-6-yl)acetate

생성물 1

HCID 86670269Methyl 2-(7-chloro-5-methyl-3-phenylpyrazolo[1,5-a]pyrimidin-6-yl)-2-hydroxyacetate수율 51%

시약·촉매·용매 1

HCID 8028
Tetrahydrofuran
용매
3회

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온도
-78 °C

실험 절차

To a stirred solution of KHMDS (0.5 M in toluene, 4.6 mL, 4.75 mmol) in THF (12 mL) at −78° C. was added a solution of methyl 2-(7-chloro-5-methyl-3-phenylpyrazolo[1,5-a]pyrimidin-6-yl)acetate (0.48 g, 1.5 mmol) in THF (12 mL) over 20 mins. The reaction mixture was stirred at −78° C. for 30 min. A solution of 3-phenyl-2-(phenylsulfonyl)-1,2-oxaziridine (0.6 g, 2.3 mmol) in THF (12 mL) was added over 10 min and the resulted reaction mixture was stirred for an additional 30 min at −78° C. The reaction mixture was quenched with saturated NH4Cl aqueous solution (2 mL). The mixture was allowed to warm up to room temperature and diluted with EtOAc (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 (250 mg, 51%). 1H-NMR (500 MHz, DMSO-d6) δ ppm 2.65 (3H, s), 3.7 (3H, s), 5.79 (1H, s), 6.62 (1H, s), 7.35-7.59 (3H, m), 8.95 (1H, s).

후처리

  1. customthe resulted reaction mixture
  2. stirringwas stirred for an additional 30 min at −78° C
  3. customThe reaction mixture was quenched with saturated NH4Cl aqueous solution (2 mL)
  4. temperatureto warm up to room temperature
  5. additiondiluted with EtOAc (100 mL)
  6. washThe organic phase was washed with water and brine
  7. dry with materialdried with sodium sulfate
  8. customThe solvent was evaporated
  9. customPurification by silica gel chromatography

출처 및 근거

ORD 기록
ord-db227adfd0f04560a01c31e47b0008b7
출처 데이터셋
uspto-grants-2014_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08633200B2

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