HCID 54434818, compound → HCID 22632139, compound
Reaction equation
[C:1]([CH2:4][N:5]1[C:11](=[O:12])[CH:10]([CH2:13][C:14]([O:16]C)=[O:15])[CH2:9][C:8]2[CH:18]=[CH:19][C:20]([O:22][CH2:23][CH2:24][CH2:25][NH:26][C:27]3[CH:32]=[CH:31][CH:30]=[CH:29][N:28]=3)=[CH:21][C:7]=2[CH2:6]1)([OH:3])=[O:2].N1C=CC=CC=1NCCCOC1C=CC2CC(CC(OCC)=O)C(=O)NCC=2C=1>O>[C:1]([CH2:4][N:5]1[C:11](=[O:12])[CH:10]([CH2:13][C:14]([OH:16])=[O:15])[CH2:9][C:8]2[CH:18]=[CH:19][C:20]([O:22][CH2:23][CH2:24][CH2:25][NH:26][C:27]3[CH:32]=[CH:31][CH:30]=[CH:29][N:28]=3)=[CH:21][C:7]=2[CH2:6]1)([OH:3])=[O:2]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
According to the procedure of Example 1(c) except substituting methyl (±)-2-(carboxymethyl)-3-oxo-8-[3-(pyridin-2-ylamino)-1-propyloxy]-2,3,4,5-tetrahydro-1H-2-benzazepine-4-acetate for the ethyl (±)-8-[3-(2-pyridylamino)-1-propyloxy]-3-oxo-2,3,4,5-tetrahydro-1H-2-benzazepine-4-acetate, the title compound (0.30 g, 56%) was prepared: MS (ES) m/e 428.4 (M+H)+. Anal. Calcd for C22H25N3O6.2 H2O: C, 57.01; H, 6.31; N, 9.07; Found: C, 57.27; H, 6.24; N, 8.86.
Sources & evidence
- ORD record
- ord-6dfc408aba8f42cbafc4059f9ddd0b45
- Source dataset
- uspto-grants-2004_11
- Patent number
- US06825188B2
Reaction notes
Loading…