2,4-Dichlorobenzoyl chloride → HCID 19833895, compound
Reaction equation
[CH:1]1[C:11]2[C:10]3[CH:12]=[CH:13][CH:14]=[CH:15][C:9]=3[CH2:8][N:7]([C:16](=[NH:20])[O:17][CH2:18][CH3:19])[CH2:6][C:5]=2[CH:4]=[CH:3][CH:2]=1.[Cl:21][C:22]1[CH:30]=[C:29]([Cl:31])[CH:28]=[CH:27][C:23]=1[C:24](Cl)=[O:25]>>[Cl:21][C:22]1[CH:30]=[C:29]([Cl:31])[CH:28]=[CH:27][C:23]=1[C:24]([N:20]=[C:16]([N:7]1[CH2:6][C:5]2[CH:4]=[CH:3][CH:2]=[CH:1][C:11]=2[C:10]2[CH:12]=[CH:13][CH:14]=[CH:15][C:9]=2[CH2:8]1)[O:17][CH2:18][CH3:19])=[O:25]Participants
3
Procedure
starting from ethyl 5,7-dihydro-6H-dibenz[c,e]azepine-6-carboximidate and 2,4-dichlorobenzoyl chloride, there is obtained ethyl N-(2,4-dichloro-benzoyl)-5,7-dihydro-6H-dibenz[c,e]azepine-6-carboximidate, m.p. 158°-159°-C.;
Sources & evidence
- ORD record
- ord-857349d1ffa845b485ee1a038cd1fd25
- Source dataset
- uspto-grants-1991_05
- Patent number
- US05015640
Reaction notes
Loading…