Hydrochloric Acid → 1-(3-Chlorophenyl)-3-[1-(3,3-dimethylazetidin-1-yl)propan-2-yl]-4-methylimidazolidin-2-one
Reaction equation
[CH3:1][C:2]1([CH3:6])[CH2:5][NH:4][CH2:3]1.Cl[CH2:8][CH:9]([N:11]1[CH:15]([CH3:16])[CH2:14][N:13]([C:17]2[CH:22]=[CH:21][CH:20]=[C:19]([Cl:23])[CH:18]=2)[C:12]1=[O:24])[CH3:10].Cl>>[Cl:23][C:19]1[CH:18]=[C:17]([N:13]2[CH2:14][CH:15]([CH3:16])[N:11]([CH:9]([CH3:10])[CH2:8][N:4]3[CH2:5][C:2]([CH3:6])([CH3:1])[CH2:3]3)[C:12]2=[O:24])[CH:22]=[CH:21][CH:20]=1Participants
4
Procedure
The title compound is prepared pursuant to the procedure of Example 4 from 3,3-dimethylazetidine and 3-(2-chloro-1-methylethyl)-1-(m-chlorophenyl)-4-methyl-2-imidazolidinone. B.p. 200° C./0.6 mm Hg. The corresponding hydrochloride melts at 162°-164° C.
Sources & evidence
- ORD record
- ord-f69a0324bc974d8f964f0cb5b12448aa
- Source dataset
- uspto-grants-1977_03
- Patent number
- US04011238
Reaction notes
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