2-Chlorobenzylamine → 2-Amino-4-(2-chloro-benzylamino)-6-furan-2-yl-pyrimidine-5-carbonitrile

HRID 1356030Notes

Reaction equation

HRID 1356030 reaction equation
[NH2:1][C:2]1[N:7]=[C:6]([C:8]2[O:9][CH:10]=[CH:11][CH:12]=2)[C:5]([C:13]#[N:14])=[C:4](S(C)=O)[N:3]=1.[Cl:18][C:19]1[CH:26]=[CH:25][CH:24]=[CH:23][C:20]=1[CH2:21][NH2:22]>COCCOC>[NH2:1][C:2]1[N:3]=[C:4]([NH:22][CH2:21][C:20]2[CH:23]=[CH:24][CH:25]=[CH:26][C:19]=2[Cl:18])[C:5]([C:13]#[N:14])=[C:6]([C:8]2[O:9][CH:10]=[CH:11][CH:12]=2)[N:7]=1

Participants

4

Reactant 2

HCID 666482-ChlorobenzylamineHCID 185076922-Amino-4-(furan-2-YL)-6-(methylsulfinyl)pyrimidine-5-carbonitrile

Product 1

HCID 99273282-Amino-4-(2-chloro-benzylamino)-6-furan-2-yl-pyrimidine-5-carbonitrile

Reagents, catalysts & solvents 1

HCID 80711,2-DimethoxyethaneSolvent

Procedure

From 2-amino-4-furan-2-yl-6-methanesulfinyl-pyrimidine-5-carbonitrile and 2-chlorobenzylamine in DME. ES-MS m/e (%): 328 (M{37Cl}+H+, 30), 326 (M{35Cl}+H+, 100).

Sources & evidence

ORD record
ord-f0a3ea0e4e8f40288ebb9ef1d590bf73
Source dataset
uspto-grants-2003_07
Patent number
US06586441B2

Reaction notes

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