Methyl 2-(3-oxocyclopentyl)acetate → {3-[3-((S)-2-Amino-1,4,5,5-tetramethyl-6-oxo-1,4,5,6-tetrahydro-pyrimidin-4-yl)-4-fluoro-phenylamino]-cyclopentyl}-acetic acid methyl ester
반응식
[NH2:1][C:2]1[N:7]([CH3:8])[C:6](=[O:9])[C:5]([CH3:11])([CH3:10])[C@:4]([C:13]2[CH:18]=[C:17]([NH2:19])[CH:16]=[CH:15][C:14]=2[F:20])([CH3:12])[N:3]=1.[CH3:21][O:22][C:23](=[O:31])[CH2:24][CH:25]1[CH2:29][CH2:28][C:27](=O)[CH2:26]1.[B][B][B][B][B][B][B][B][B][B]>>[CH3:21][O:22][C:23](=[O:31])[CH2:24][CH:25]1[CH2:29][CH2:28][CH:27]([NH:19][C:17]2[CH:16]=[CH:15][C:14]([F:20])=[C:13]([C@:4]3([CH3:12])[C:5]([CH3:10])([CH3:11])[C:6](=[O:9])[N:7]([CH3:8])[C:2]([NH2:1])=[N:3]3)[CH:18]=2)[CH2:26]1참가 물질
4
반응물 3
생성물 1
실험 절차
The reductive amination of (S)-2-amino-6-(5-amino-2-fluoro-phenyl)-3,5,5,6-tetramethyl-5,6-dihydro-3H-pyrimidin-4-one (intermediate J) and (3-oxo-cyclopentyl)-acetic acid methyl ester using decaborane yielded a mixture of isomers of the title compound as a white foam. MS (ESI): m/z=419.3 [M+H]+.
후처리
- customyielded
출처 및 근거
- ORD 기록
- ord-a8a2bb4bc5784bb180245fb32ea1f5f2
- 출처 데이터셋
- uspto-grants-2014_08
- 특허 번호
- US08815881B2
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