Chemical Compound

(2R,5R)-tert-butyl 5- (cyanomethyl)-5-(3-((4- (methylsulfonyl)phenyl) amino)-4-oxo-4,5- dihydro-1H-pyrazolo [4,3-c]pyridin-1-yl) tetrahydro-2H-pyran-2- carboxylate (from Example 5-36) Chiral separation of free pyridone using LC column, IB column, 40% MeOH/EtOH = 3:2, 60% heptanes, Tr = 9.6 minutes.

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(2R,5R)-tert-butyl 5- (cyanomethyl)-5-(3-((4- (methylsulfonyl)phenyl) amino)-4-oxo-4,5- dihydro-1H-pyrazolo [4,3-c]pyridin-1-yl) tetrahydro-2H-pyran-2- carboxylate (from Example 5-36) Chiral separation of free pyridone using LC column, IB column, 40% MeOH/EtOH = 3:2, 60% heptanes, Tr = 9.6 minutes. 结构式
Primary record

(2R,5R)-tert-butyl 5- (cyanomethyl)-5-(3-((4- (methylsulfonyl)phenyl) amino)-4-oxo-4,5- dihydro-1H-pyrazolo [4,3-c]pyridin-1-yl) tetrahydro-2H-pyran-2- carboxylate (from Example 5-36) Chiral separation of free pyridone using LC column, IB column, 40% MeOH/EtOH = 3:2, 60% heptanes, Tr = 9.6 minutes.

库存
550 克
纯度
98.1 %

化合物标识与属性

PubChem CID
146011760
SMILES
CC(C)(C)OC(=O)[C@H]1CC[C@](CO1)(CC#N)N2C3=CC=NC(=O)C3C(=NC4=CC=C(C=C4)S(=O)(=O)C)N2
Canonical SMILES
CC(C)(C)OC(=O)[C@H]1CC[C@](CC#N)(N2NC(=Nc3ccc(S(C)(=O)=O)cc3)C3C(=O)N=CC=C32)CO1

名称与同义词

  • BDBM390969
  • US9957264, Example 5-40
  • (2R,5R)-tert-butyl 5- (cyanomethyl)-5-(3-((4- (methylsulfonyl)phenyl) amino)-4-oxo-4,5- dihydro-1H-pyrazolo [4,3-c]pyridin-1-yl) tetrahydro-2H-pyran-2- carboxylate (from Example 5-36) Chiral separation of free pyridone using LC column, IB column, 40% MeOH/EtOH = 3:2, 60% heptanes, Tr = 9.6 minutes.