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Acetic Acid → 2-methylthio-5,6,7,9-tetrahydrothiopyrano[3,4-d]-1,2,4-triazolo[1,5-a]pyrimidine-5(10H)-one

HRID 973544
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반응식

HRID 973544 반응식
[NH2:1][C:2]1[NH:6][N:5]=[C:4]([S:7][CH3:8])[N:3]=1.O=[C:10]1[CH:15]([C:16](OCC)=O)[CH2:14][CH2:13][S:12][CH2:11]1.C(O)(=[O:23])C>>[CH3:8][S:7][C:4]1[N:3]=[C:2]2[N:1]=[C:14]3[C:13](=[O:23])[S:12][CH2:11][CH:10]=[C:15]3[CH2:16][N:6]2[N:5]=1
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참가 물질

4

반응물 3

HCID 176Acetic AcidHCID 784713-(Methylthio)-1,2,4-triazol-5-amineHCID 15049900Ethyl 3-oxothiane-4-carboxylate

생성물 1

HCID 199886062-methylthio-5,6,7,9-tetrahydrothiopyrano[3,4-d]-1,2,4-triazolo[1,5-a]pyrimidine-5(10H)-one수율 62.9%

실험 절차

0.976 g (0.0075 mole) of 5-amino-3-methylthio-1H-1,2,4-triazole are dissolved in 6 ml of acetic acid, then 1.368 g (0.075 mole) of ethyl 3-oxo-3,4,5,6-tetrahydro-2H-thiopyrane-4-carboxylate are added and the reaction mixture is boiled for 30 minutes. The precipitated product is filtered off from the hot solution, washed with water and recrystallized from dimethylformamide. Thus 1.2 g (62.9%) of 2-methylthio-5,6,7,9-tetrahydrothiopyrano[3,4-d]-1,2,4-triazolo[1,5-a]pyrimidine-5(10H)-one are obtained which melt at 294°-297° C.

후처리

  1. filtrationThe precipitated product is filtered off from the hot solution
  2. washwashed with water
  3. customrecrystallized from dimethylformamide

출처 및 근거

ORD 기록
ord-31cd5683d5e74ad18d5d2d1373a505dc
출처 데이터셋
uspto-grants-1991_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05064826

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