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Ammonia → HCID 89650994, 화합물

HRID 515939
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HRID 515939 반응식
C([O:9][C@H:10]1[C@:14]([F:16])([CH3:15])[C@H:13]([N:17]2[CH:22]=[CH:21][C:20](=[O:23])[NH:19][C:18]2=[O:24])[O:12][C@@:11]1([F:34])[CH2:25]C(=O)C1C=CC=CC=1)(=O)C1C=CC=CC=1.N.C[OH:37]>>[F:16][C@:14]1([CH3:15])[C@H:10]([OH:9])[C@@:11]([F:34])([CH2:25][OH:37])[O:12][C@H:13]1[N:17]1[CH:22]=[CH:21][C:20](=[O:23])[NH:19][C:18]1=[O:24]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 222AmmoniaHCID 887Methanol2회HCID 131733327HCID 131733327, 화합물

생성물 1

HCID 89650994HCID 89650994, 화합물수율 38%

실험 절차

Chiral (2R,3S,4R,5R)-5-(2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)-2,4-difluor-O-2-benzoylmethyl-4-methyl-tetrahydrofuran-3-yl benzoate (0.34 g, 0.7 mmol) was dissolved into methanol, and a solution of ammonia in methanol (7 N, 20 mL) was added. The reaction mixture was stirred at room temperature for overnight. The mixture was concentrated, and the residue was purified by silica gel column chromatography (DCM:MeOH=20:1) and pre-HPLC to afford the title compound as a white solid (0.074 g, 38%).

후처리

  • concentrationThe mixture was concentrated
  • customthe residue was purified by silica gel column chromatography (DCM:MeOH=20:1)
  • 출처 및 근거

    ORD 기록
    ord-30de34eda843420395b4a164d783dc16
    출처 데이터셋
    uspto-grants-2015_08
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US09108999B2

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