Reaction equation
Br[C:2]1[CH:14]=[C:13]2[C:5]([C:6]3[C:7](=[O:23])[C:8]4[CH:20]=[CH:19][C:18]([O:21][CH3:22])=[CH:17][C:9]=4[C:10]([CH3:16])([CH3:15])[C:11]=3[NH:12]2)=[CH:4][CH:3]=1.COC1C=C2C(CCC(=O)C2(C)C)=CC=1.Cl.[Cl:40]C1C=C(NN)C=CC=1>>[Cl:40][C:2]1[CH:14]=[C:13]2[C:5]([C:6]3[C:7](=[O:23])[C:8]4[CH:20]=[CH:19][C:18]([O:21][CH3:22])=[CH:17][C:9]=4[C:10]([CH3:16])([CH3:15])[C:11]=3[NH:12]2)=[CH:4][CH:3]=1Participants
4
Procedure
Under the same conditions as the method for synthesizing Compound A3-1 and Compound A4, the title compound was prepared as a crude product from Compound A2 and (3-chlorophenyl)-hydrazine hydrochloric acid salt.
Sources & evidence
- ORD record
- ord-0f35be01de184ffbb4a7bc8c5d9114eb
- Source dataset
- uspto-grants-2016_09
- Patent number
- US09440922B2
Linked notes
Loading…