N,N-Dimethylaminoethyl chloride hydrochloride → 2-(2-Dimethylaminoethylamino)-4-methyl-6-dimethylaminopyrimidine
Reaction equation
[C:1]([NH:4][C:5]1[N:10]=[C:9]([CH3:11])[CH:8]=[C:7]([N:12]([CH3:14])[CH3:13])[N:6]=1)(=O)[CH3:2].Cl.[CH3:16][N:17](C)[CH2:18]CCl>>[CH3:16][N:17]([CH3:18])[CH2:2][CH2:1][NH:4][C:5]1[N:10]=[C:9]([CH3:11])[CH:8]=[C:7]([N:12]([CH3:14])[CH3:13])[N:6]=1Participants
3
Procedure
Following the procedure of Example 1, Part A 2-acetamido-4-methyl-6-dimethylaminopyrimidine and 2-dimethylaminoethyl chloride hydrochloride, 2-(2-dimethylaminoethylamino)-4-methyl-6-dimethylaminopyrimidine is obtained with a boiling point of 120°-124° C. at 0.03 mm.
Sources & evidence
- ORD record
- ord-013002db66694c59b939ac9725818c8d
- Source dataset
- uspto-grants-1980_07
- Patent number
- US04215121
Reaction notes
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