Hydrochloric Acid → HCID 13355638, compound
Reaction equation
Cl.Cl.[NH2:3][C:4]1[C:9]([C:10]([F:13])([F:12])[F:11])=[CH:8][C:7]([C:14](=[O:20])[CH2:15][NH:16][CH:17]([CH3:19])[CH3:18])=[CH:6][C:5]=1[Br:21].[BH4-].[Na+]>>[NH2:3][C:4]1[C:9]([C:10]([F:11])([F:12])[F:13])=[CH:8][C:7]([CH:14]([OH:20])[CH2:15][NH:16][CH:17]([CH3:18])[CH3:19])=[CH:6][C:5]=1[Br:21]Participants
4
Procedure
m.p. 102°-103° C., m.p. of the hydrochloride: 177°-179° C. (decomp.), was prepared from 4'-amino-3'-bromo-2-isopropylamino-5'-trifluoromethyl-acetophenone hydrochloride and sodium borohydride analogous to Example 1.
Sources & evidence
- ORD record
- ord-8df0241783cd4903ae0c203a874d0a67
- Source dataset
- uspto-grants-1978_10
- Patent number
- US04119710
Reaction notes
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