Hydrochloric Acid → HCID 13355593, compound
Reaction equation
Cl.[NH2:2][C:3]1[C:8]([F:9])=[CH:7][C:6]([C:10](=[O:18])[CH2:11][NH:12][C:13]([CH2:16][CH3:17])([CH3:15])[CH3:14])=[CH:5][C:4]=1[C:19]#[N:20]>>[NH2:2][C:3]1[C:8]([F:9])=[CH:7][C:6]([CH:10]([OH:18])[CH2:11][NH:12][C:13]([CH2:16][CH3:17])([CH3:14])[CH3:15])=[CH:5][C:4]=1[C:19]#[N:20]Participants
3
Procedure
m.p. of the hydrochloride: 172°-175° C. (decomp.)., was prepared from 4'-amino-3'-cyano-5'-fluoro-2-tert.pentylaminoacetophenone analogous to Example 49.
Sources & evidence
- ORD record
- ord-b650e28840f34af0989a039ed766b141
- Source dataset
- uspto-grants-1978_10
- Patent number
- US04119710
Reaction notes
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