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Phosphorus sulfide (P2S5) → HCID 20494272, 화합물

HRID 1075157
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HRID 1075157 반응식
[Cl:1][C:2]1[C:3](=O)[NH:4][C:5](=[O:9])[NH:6][C:7]=1[CH3:8].P12(SP3(SP(SP(S3)(S1)=S)(=S)S2)=S)=[S:12]>O1CCOCC1>[Cl:1][C:2]1[C:3](=[S:12])[NH:4][C:5](=[O:9])[NH:6][C:7]=1[CH3:8]
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참가 물질

4

반응물 2

HCID 14817Phosphorus sulfide (P2S5)HCID 952682,4(1H,3H)-Pyrimidinedione, 5-chloro-6-methyl-

생성물 1

HCID 20494272HCID 20494272, 화합물수율 75%

시약·촉매·용매 1

HCID 312751,4-Dioxane용매

실험 절차

5-Chloro-6-methyluracil (prepared as described in Johnson, B. T. J. Amer. Chem. Soc. 65 (1943) (1220) (0.018 mol) and phosphorus pentasulphide (0.019 mol) were heated together in refluxing dioxan (200 ml) for 45 min. The hot reaction mixture was then filtered and the cold filtrate concentrated and diluted with ether. The participate collected after a few hours in the cold, was recrystallised from water; yield 75% m.p. 297°-300° C. (decomp.); (Found: C, 32.69; H, 3.96. Calc. for C5H5ClN2OS.1/2H2O: C, 32.35; H, 3.25).

후처리

  1. filtrationThe hot reaction mixture was then filtered
  2. concentrationthe cold filtrate concentrated
  3. additiondiluted with ether
  4. customThe participate collected after a few hours in the cold,
  5. customwas recrystallised from water

출처 및 근거

ORD 기록
ord-4144011a89304f38a047939c568a2deb
출처 데이터셋
uspto-grants-1983_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04395406

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