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Phosphorus oxychloride → Methyl 2-(7-chloro-5-methyl-2-phenylpyrazolo[1,5-A]pyrimidin-6-YL)acetate

HRID 574322
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반응식

HRID 574322 반응식
[CH3:1][C:2]1[NH:3][C:4]2[N:5]([N:14]=[C:15]([C:17]3[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=3)[CH:16]=2)[C:6](=O)[C:7]=1[CH2:8][C:9]([O:11][CH3:12])=[O:10].O=P(Cl)(Cl)[Cl:25]>>[Cl:25][C:6]1[N:5]2[N:14]=[C:15]([C:17]3[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=3)[CH:16]=[C:4]2[N:3]=[C:2]([CH3:1])[C:7]=1[CH2:8][C:9]([O:11][CH3:12])=[O:10]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 24813Phosphorus oxychlorideHCID 178499519HCID 178499519, 화합물

생성물 1

HCID 71742099Methyl 2-(7-chloro-5-methyl-2-phenylpyrazolo[1,5-A]pyrimidin-6-YL)acetate수율 86.9%

실험 절차

To methyl 2-(5-methyl-7-oxo-2-phenyl-4,7-dihydropyrazolo[1,5-a]pyrimidin-6-yl)acetate (3 g, 10.09 mmol) was added POCl3 (25 mL, 268 mmol). The reaction mixture was heated at reflux for 1 h. After cooling, the reaction mixture was added drop-wise to ice-water. A brown solid precipitated. The solid was filtered and washed with water, then dissolved in ethyl acetate. The organic solution was washed with saturated NaHCO3 and dried over sodium sulfate. The solvent was evaporated to give the title compound (2.77 g, 84%). 1H-NMR (400 MHz, DMSO-d6) δ 2.58 (3H, s), 3.71 (3 H, s), 4.04 (2 H, s), 7.29 (1 H, s), 7.43-7.58 (3 H, m), 8.07 (2 H, d, J=7.0 Hz).

후처리

  1. temperature
The reaction mixture was heated
  • temperatureat reflux for 1 h
  • temperatureAfter cooling
  • customA brown solid precipitated
  • filtrationThe solid was filtered
  • washwashed with water
  • dissolutiondissolved in ethyl acetate
  • washThe organic solution was washed with saturated NaHCO3
  • dry with materialdried over sodium sulfate
  • customThe solvent was evaporated
  • 출처 및 근거

    ORD 기록
    ord-038dd61cc086482b8517aed8790d1e2f
    출처 데이터셋
    uspto-grants-2015_05
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US09034882B2

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