Hydrochloric Acid → HCID 13355694, compound
Reaction equation
Cl.[NH2:2][C:3]1[C:8]([C:9]#[N:10])=[CH:7][C:6]([C:11](=[O:19])[CH2:12][NH:13][CH:14]2[CH2:18][CH2:17][CH2:16][CH2:15]2)=[CH:5][C:4]=1[C:20]#[N:21]>>[NH2:2][C:3]1[C:8]([C:9]#[N:10])=[CH:7][C:6]([CH:11]([OH:19])[CH2:12][NH:13][CH:14]2[CH2:15][CH2:16][CH2:17][CH2:18]2)=[CH:5][C:4]=1[C:20]#[N:21]Participants
3
Procedure
m.p. of the hydrochloride: 214°-216° C., was prepared from 4'-amino-2-cyclopentylamino-3',5'-dicyano-acetophenone analogous to Example 48.
Sources & evidence
- ORD record
- ord-0d20452708e24864a5728037827768a1
- Source dataset
- uspto-grants-1978_10
- Patent number
- US04119710
Reaction notes
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