반응식
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([C@:8]2([O:17][C@H:16]([CH2:18][OH:19])[C@@H:14]([OH:15])[C@H:12]([OH:13])[C@H:10]2[OH:11])[OH:9])=[CH:4][C:3]=1[CH2:20][C:21]1[CH:26]=[CH:25][C:24](OS(C(F)(F)F)(=O)=O)=[CH:23][CH:22]=1.[C:35]([C:37]1[CH:38]=[N:39][CH:40]=[CH:41][CH:42]=1)#[CH:36]>>[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([C@:8]2([O:17][C@H:16]([CH2:18][OH:19])[C@@H:14]([OH:15])[C@H:12]([OH:13])[C@H:10]2[OH:11])[OH:9])=[CH:4][C:3]=1[CH2:20][C:21]1[CH:26]=[CH:25][C:24]([C:36]#[C:35][C:37]2[CH:38]=[N:39][CH:40]=[CH:41][CH:42]=2)=[CH:23][CH:22]=1참가 물질
3
실험 절차
The compound was obtained starting from 1-chloro-4-(β-D-glucopyranos-1-yl)-2-(4-trifluoromethylsulfonyloxy-benzyl)-benzene and 3-ethynyl-pyridine.
후처리
- customThe compound was obtained
출처 및 근거
- ORD 기록
- ord-34ef5a8978d740b7bc440277e489dfe1
- 출처 데이터셋
- uspto-grants-2010_08
- 특허 번호
- US07772378B2
연결된 노트
불러오는 중…