Hydrochloric Acid → HCID 13355648, 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:21])[CH2:15][NH:16][C:17]([CH3:20])([CH3:19])[CH3:18])=[CH:6][C:5]=1[Br:22].[BH4-].[Na+]>>[NH2:3][C:4]1[C:9]([C:10]([F:11])([F:12])[F:13])=[CH:8][C:7]([CH:14]([OH:21])[CH2:15][NH:16][C:17]([CH3:18])([CH3:19])[CH3:20])=[CH:6][C:5]=1[Br:22]Participants
4
Procedure
m.p. 85°-87° C., m.p. of the hydrochloride: 205°-206° C. (decomp.), was prepared from 4'-amino-3'-bromo-2-tert. butylamino-5'-trifluoromethyl-acetophenone hydrochloride and sodium borohydride analogous to Example 1.
Sources & evidence
- ORD record
- ord-30538706546044399cd8c6d054ac8a26
- Source dataset
- uspto-grants-1978_10
- Patent number
- US04119710
Reaction notes
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