3-Methylpyrrolidin-3-ol → HCID 89538970, 화합물
반응식
[CH2:1]([N:8]1[C:12]2[N:13]=[C:14]([C:23]([CH3:26])([CH3:25])[CH3:24])[N:15]=[C:16]([N:17]3[CH2:21][CH2:20][C@@H:19]([OH:22])[CH2:18]3)[C:11]=2[N:10]=[N:9]1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[CH2:27]([N:34]1[C:38]2[N:39]=[C:40]([C:44]([CH3:47])([CH3:46])[CH3:45])[N:41]=[C:42](Cl)[C:37]=2[N:36]=[N:35]1)[C:28]1[CH:33]=[CH:32][CH:31]=[CH:30][CH:29]=1.[CH3:48][C:49]1([OH:54])[CH2:53][CH2:52][NH:51][CH2:50]1>>[CH2:1]([N:8]1[C:12]2[N:13]=[C:14]([C:23]([CH3:26])([CH3:25])[CH3:24])[N:15]=[C:16]([N:17]3[CH2:21][CH2:20][C:19]([CH3:27])([OH:22])[CH2:18]3)[C:11]=2[N:10]=[N:9]1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[CH2:27]([N:34]1[C:38]2[N:39]=[C:40]([C:44]([CH3:47])([CH3:46])[CH3:45])[N:41]=[C:42]([N:51]3[CH2:52][CH2:53][C@:49]([CH3:48])([OH:54])[CH2:50]3)[C:37]=2[N:36]=[N:35]1)[C:28]1[CH:33]=[CH:32][CH:31]=[CH:30][CH:29]=1.[CH2:1]([N:8]1[C:12]2[N:13]=[C:14]([C:23]([CH3:26])([CH3:25])[CH3:24])[N:15]=[C:16]([N:17]3[CH2:21][CH2:20][C@@:19]([CH3:27])([OH:22])[CH2:18]3)[C:11]=2[N:10]=[N:9]1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1참가 물질
6
반응물 3
생성물 3
실험 절차
In analogy to the procedure described for the synthesis of (R)-1-(3-Benzyl-5-tert-butyl-3H-[1,2,3]triazolo[4,5-d]pyrimidin-7-yl)-pyrrolidin-3-ol (example 113, a) the title compound was prepared from 3-benzyl-5-tert-butyl-7-chloro-triazolo[4,5-d]pyrimidine and 3-Methyl-pyrrolidin-3-ol and subjected to separation by chiral HPLC to yield (S)-1-(3-benzyl-5-tert-butyl-3H-[1,2,3]triazolo[4,5-d]pyrimidin-7-yl)-3-methylpyrrolidin-3-ol and (R)-1-(3-benzyl-5-tert-butyl-3H-[1,2,3]triazolo[4,5-d]pyrimidin-7-yl)-3-methylpyrrolidin-3-ol. The enantiopure intermediates where isolated with 39% and 36% yield.
후처리
- customsubjected to separation by chiral HPLC
출처 및 근거
- ORD 기록
- ord-a90d477f97e24abdaa46b49ce2f605e9
- 출처 데이터셋
- uspto-grants-2015_06
- 특허 번호
- US09067943B2
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