Hydrochloric Acid → HCID 22765868, 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][N:13]([OH:18])[C:14]([CH3:17])([CH3:16])[CH3:15])=[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][N:13]([OH:18])[C:14]([CH3:17])([CH3:15])[CH3:16])=[CH:5][C:4]=1[C:20]#[N:21]Participants
3
Procedure
m.p. of the hydrochloride: 240°-241° C. (decomp.), was prepared from 4'-amino-3',5'-dicyano-2-(hydroxy-tert.butylamino)-acetophenone analogous to Example 48.
Sources & evidence
- ORD record
- ord-d3e668b508eb450a9bceec2c98ec4f10
- Source dataset
- uspto-grants-1978_10
- Patent number
- US04119710
Reaction notes
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