Hydrochloric Acid → 1-(4'-Amino-3',5'-dicyano-phenyl)-2-tert.butylamino-ethanol
Reaction equation
Cl.[NH2:2][C:3]1[C:8]([C:9]#[N:10])=[CH:7][C:6]([C:11](=[O:18])[CH2:12][NH:13][C:14]([CH3:17])([CH3:16])[CH3:15])=[CH:5][C:4]=1[C:19]#[N:20]>>[NH2:2][C:3]1[C:4]([C:19]#[N:20])=[CH:5][C:6]([CH:11]([OH:18])[CH2:12][NH:13][C:14]([CH3:15])([CH3:16])[CH3:17])=[CH:7][C:8]=1[C:9]#[N:10]Participants
3
Procedure
m.p. of the hydrochloride: 251°-253° C. (decomp.), was prepared from 4'-amino-2-tert.butylamino-3',5'-dicyano-acetophenone analogous to Example 48.
Sources & evidence
- ORD record
- ord-78b4a3ee2fb5452e8d2011ef38adcb05
- Source dataset
- uspto-grants-1978_10
- Patent number
- US04119710
Reaction notes
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