Hydrochloric Acid → HCID 13355564, compound
Reaction equation
Cl.[NH2:2][C:3]1[C:8]([F:9])=[CH:7][C:6]([C:10](=[O:19])[CH2:11][NH:12][CH:13]2[CH2:18][CH2:17][CH2:16][CH2:15][CH2:14]2)=[CH:5][C:4]=1[Br:20].[BH4-].[Na+]>>[NH2:2][C:3]1[C:8]([F:9])=[CH:7][C:6]([CH:10]([OH:19])[CH2:11][NH:12][CH:13]2[CH2:18][CH2:17][CH2:16][CH2:15][CH2:14]2)=[CH:5][C:4]=1[Br:20]Participants
4
Procedure
m.p. of the hydrochloride: 191°-195° C. (decomp.), was prepared from 4'-amino-3'-bromo-2-cyclohexylamino-5'-fluoroacetophenone and sodium borohydride analogous to Example 49.
Sources & evidence
- ORD record
- ord-7ceb24a077504ad3b496e0c23cb76d5a
- Source dataset
- uspto-grants-1978_10
- Patent number
- US04119710
Reaction notes
Loading…