Chloride → HCID 19699089, compound
Reaction equation
[Cl:1][C:2]1[CH:23]=[C:22]([N+:24]([O-])=O)[CH:21]=[CH:20][C:3]=1[C:4]([N:6]1[CH2:12][C:11]2[CH:13]=[CH:14][S:15][C:10]=2[CH2:9][C:8]2[N:16]=[CH:17][CH:18]=[CH:19][C:7]1=2)=[O:5].[Cl-]>C(O)C>[Cl:1][C:2]1[CH:23]=[C:22]([NH2:24])[CH:21]=[CH:20][C:3]=1[C:4]([N:6]1[CH2:12][C:11]2[CH:13]=[CH:14][S:15][C:10]=2[CH2:9][C:8]2[N:16]=[CH:17][CH:18]=[CH:19][C:7]1=2)=[O:5]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
As described for Reference Example 204 5-(2-chloro-4-nitrobenzoyl)-4,10-dihydro-5H-pyrido[3,2-b]-thieno[2,3-e]azepine is reduced with stannus chloride (SnCl2) in ethanol to give the product as a solid.
Sources & evidence
- ORD record
- ord-1b29c15a742f406aadf108d22c94ec92
- Source dataset
- uspto-grants-1998_02
- Patent number
- US05719278
Reaction notes
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