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Ammonia → HCID 68190285, 화합물

HRID 513775
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HRID 513775 반응식
C[O:2][C:3]([C:5]1[CH:22]=[C:21]2[C:8]([S:9](=[O:24])(=[O:23])[NH:10][C:11]3[C:20]2=[CH:19][CH:18]=[C:17]2[C:12]=3[N:13]=[CH:14][CH:15]=[CH:16]2)=[CH:7][CH:6]=1)=O.[NH3:25]>CO>[O:23]=[S:9]1(=[O:24])[C:8]2[C:21](=[CH:22][C:5]([C:3]([NH2:25])=[O:2])=[CH:6][CH:7]=2)[C:20]2[C:11](=[C:12]3[C:17](=[CH:18][CH:19]=2)[CH:16]=[CH:15][CH:14]=[N:13]3)[NH:10]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 222AmmoniaHCID 60164307HCID 60164307, 화합물

생성물 1

HCID 68190285HCID 68190285, 화합물수율 17%

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

A solution of 6,6-dioxo-5,6-dihydro-6λ*6*-thia-4,5-diaza-chrysene-9-carboxylic acid methyl ester 307 (50 mg, 0.15 mmol) in 7M NH3 in MeOH (5 ml) was heated at 90 C in sealed tube for 36 h. After cooling, the mixture was concentrated in vacuo. The crude residue was purified by column chromatography with DCM/MeOH (95:5) as the eluent to give the title compound (8 mg, 17%).

후처리

  1. temperatureAfter cooling
이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트
  • concentrationthe mixture was concentrated in vacuo
  • customThe crude residue was purified by column chromatography with DCM/MeOH (95:5) as the eluent
  • 출처 및 근거

    ORD 기록
    ord-c834d31477924911b95016ab085fc345
    출처 데이터셋
    uspto-grants-2015_08
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US09102688B2

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