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Phosphorus oxychloride → HCID 86707952, 화합물

HRID 1526491
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HRID 1526491 반응식
O[C:2]1[C:3]2[C:4]3[CH:5]=[C:6]([CH2:15][C:16]([O:18][CH2:19][CH3:20])=[O:17])[CH:7]=[CH:8][C:9]=3[S:10][C:11]=2[N:12]=[CH:13][N:14]=1.O=P(Cl)(Cl)[Cl:23]>>[Cl:23][C:2]1[C:3]2[C:4]3[CH:5]=[C:6]([CH2:15][C:16]([O:18][CH2:19][CH3:20])=[O:17])[CH:7]=[CH:8][C:9]=3[S:10][C:11]=2[N:12]=[CH:13][N:14]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 24813Phosphorus oxychlorideHCID 178470648HCID 178470648, 화합물

생성물 1

HCID 86707952HCID 86707952, 화합물수율 72%

실험 절차

A solution of ethyl 2-[3-hydroxy-8-thia-4,6-diazatricyclo[7.4.0.0^[2,7]]trideca-1(9),2(7),3,5,10,12-hexaen-12-yl]acetate (2.10 g, 7.28 mmol, 1.00 equiv) in POCl3 (23 mL) was stirred for 1 h at 90° C. in an oil bath. The reaction mixture was cooled to room temperature and concentrated under reduced pressure. The residue dissolved in EtOAc was poured into a cooled saturated aqueous sodium bicarbonate, extracted with ethyl acetate. The combined organic layers were washed with brine, dried over sodium sulfate and concentrated in vacuo. The residue was purified by a silica gel column chromatography with ethyl acetate/petroleum ether (1:5) to afford ethyl 2-[3-chloro-8-thia-4,6-diazatricyclo[7.4.0.0^[2,7]]trideca-1(9),2(7),3,5,10,12-hexaen-12-yl]acetate (1.61 g, 72%) as a white solid. LCMS (ES, m/z): 307 and 309 (M+H+).

후처리

  1. concentration
concentrated under reduced pressure
  • dissolutionThe residue dissolved in EtOAc
  • additionwas poured into a cooled saturated aqueous sodium bicarbonate
  • extractionextracted with ethyl acetate
  • washThe combined organic layers were washed with brine
  • dry with materialdried over sodium sulfate
  • concentrationconcentrated in vacuo
  • customThe residue was purified by a silica gel column chromatography with ethyl acetate/petroleum ether (1:5)
  • 출처 및 근거

    ORD 기록
    ord-6a3750ef82444c65bac794587987b169
    출처 데이터셋
    uspto-grants-2015_07
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US09085586B2

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