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Phosphorus oxychloride → Methyl 5-(acetoxymethyl)-7-chloro-s-triazolo[1,5-a]pyrimidine-2-carboxylate

HRID 1755901
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인쇄 미리보기

반응식

HRID 1755901 반응식
[C:1]([O:4][CH2:5][C:6]1[NH:7][C:8]2[N:9]([N:13]=[C:14]([C:16]([O:18][CH3:19])=[O:17])[N:15]=2)[C:10](=O)[CH:11]=1)(=[O:3])[CH3:2].P(Cl)(Cl)([Cl:22])=O>>[C:1]([O:4][CH2:5][C:6]1[CH:11]=[C:10]([Cl:22])[N:9]2[N:13]=[C:14]([C:16]([O:18][CH3:19])=[O:17])[N:15]=[C:8]2[N:7]=1)(=[O:3])[CH3:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 24813Phosphorus oxychlorideHCID 178499056HCID 178499056, 화합물

생성물 1

HCID 19917996Methyl 5-(acetoxymethyl)-7-chloro-s-triazolo[1,5-a]pyrimidine-2-carboxylate

실험 절차

A suspension of 100 mg (0.38 mmol) of methyl 5-(acetoxymethyl)-4,7-dihydro-7-oxo-s-triazolo[1,5-a]pyrimidine-2-carboxylate in 7 ml of phosphorus oxychloride is held under reflux for 6 hours and subsequently concentrated in a vacuum. The residue is dissolved in dichloromethane. The solution is washed with ice/water, dried over sodium sulphate and concentrated. After crystallization from methanol/diethyl ether there are obtained 70 mg of methyl 5-(acetoxymethyl)-7-chloro-s-triazolo[1,5-a]pyrimidine-2-carboxylate as brown crystals of melting point 120° C.

후처리

  1. temperatureunder reflux for 6 hours
  2. concentrationsubsequently concentrated in a vacuum
  3. dissolution
The residue is dissolved in dichloromethane
  • washThe solution is washed with ice/water
  • dry with materialdried over sodium sulphate
  • concentrationconcentrated
  • customAfter crystallization from methanol/diethyl ether there
  • 출처 및 근거

    ORD 기록
    ord-794372755fbd40989ee2f05abbe9e769
    출처 데이터셋
    uspto-grants-1995_08
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US05438052

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