Nitrogen → [2-(2-dihydroxymethyl-oxazol-4-ylmethyl)-2H-[1,2,3]triazol-4-yl]-carbamic acid 2-chloro-benzyl ester
반응식
N#N.[Cl:3][C:4]1[CH:27]=[CH:26][CH:25]=[CH:24][C:5]=1[CH2:6][O:7][C:8](=[O:23])[NH:9][C:10]1[CH:14]=[N:13][N:12]([CH2:15][C:16]2[N:17]=[C:18]([CH2:21][OH:22])[O:19][CH:20]=2)[N:11]=1.C(C#N)(C)=[O:29]>O=[Mn]=O>[Cl:3][C:4]1[CH:27]=[CH:26][CH:25]=[CH:24][C:5]=1[CH2:6][O:7][C:8](=[O:23])[NH:9][C:10]1[CH:14]=[N:13][N:12]([CH2:15][C:16]2[N:17]=[C:18]([CH:21]([OH:29])[OH:22])[O:19][CH:20]=2)[N:11]=1참가 물질
5
반응물 3
생성물 1
시약·촉매·용매 1
실험 절차
In a flame dried round-bottomed flask equipped with a magnetic stir bar and under inert atmosphere (N2), a solution of [2-(2-hydroxymethyl-oxazol-4-ylmethyl)-2H-[1,2,3]triazol-4-yl]-carbamic acid 2-chloro-benzyl ester (37 mg, 0.10 mmol) in AcCN (3.0 mL) was treated at rt with MnO2 (49 mg, 0.51 mmol) and the reaction mixture was stirred at rt for 16 h before being filtered through Celite. The solvent was removed under reduced pressure to give the title compound as a brown solid. TLC: rf (EA)=0.48. LC-MS-conditions 02: tR=0.83 min; [M+H]+=380.69.
후처리
- filtrationbefore being filtered through Celite
- customThe solvent was removed under reduced pressure
출처 및 근거
- ORD 기록
- ord-9afd8c0694ef4be3984c234fc056e9eb
- 출처 데이터셋
- uspto-grants-2013_09
- 특허 번호
- US08536209B2
반응 노트
불러오는 중…