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Azane;hydrate → HCID 14653250, 화합물

HRID 893305
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HRID 893305 반응식
[Cl:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[N:8]1[C:13](=[O:14])[C:12]2[CH:15]=[C:16]([S:18](Cl)(=[O:20])=[O:19])[S:17][C:11]=2[N:10]=[C:9]1[CH3:22].O.[NH3:24]>O1CCCC1>[Cl:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[N:8]1[C:13](=[O:14])[C:12]2[CH:15]=[C:16]([S:18](=[O:20])(=[O:19])[NH2:24])[S:17][C:11]=2[N:10]=[C:9]1[CH3:22]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 12896473Azane;hydrateHCID 14653249HCID 14653249, 화합물

생성물 1

HCID 14653250HCID 14653250, 화합물

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

In 200 ml of tetrahydrofuran was suspended 23 g of 3,4-dihydro-3-(2-chlorophenyl)-6-chlorosulfonyl-2-methyl-4-oxothieno[2,3-d]pyrimidine, and this suspension was poured onto 200 ml of ammonia water at one time. The mixture was stirred at room temperature for 40 minutes. The reaction mixture was concentrated, and water was added to the residue. The crystals were collected by suction-filtration to afford 15.8 g of the title compound, m.p. 251° C.

후처리

  • concentrationThe reaction mixture was concentrated
  • additionwater was added to the residue
  • filtrationThe crystals were collected by suction-filtration
  • 출처 및 근거

    ORD 기록
    ord-04361305d37c46f8bd57daf3a944b26f
    출처 데이터셋
    uspto-grants-1992_06
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US05124331

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