Benzoyl chloride → HCID 12611968, compound
Reaction equation
[NH2:1][C:2]1[C:3]([Cl:9])=[N:4][CH:5]=[N:6][C:7]=1[Cl:8].[C:10](Cl)(=[O:17])[C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1>>[Cl:9][C:3]1[C:2]([NH:1][C:10](=[O:17])[C:11]2[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=2)=[C:7]([Cl:8])[N:6]=[CH:5][N:4]=1Participants
3
Conditions
- Temperature
- 100 °C
Procedure
A mixture of 5-amino-4,6-dichloropyrimidine (1.15 g, 0.00701 mol) and benzoyl chloride (1.0 mL, 0.0086 mol) was heated at 100° C. overnight. The reaction was cooled and the residue was triturated with diethyl ether, filtered and collected to obtain 1.6 g (85%).
Workup
- temperatureThe reaction was cooled
- customthe residue was triturated with diethyl ether
- filtrationfiltered
- customcollected
- customto obtain 1.6 g (85%)
Sources & evidence
- ORD record
- ord-e4f6c3a256b54b84a1d98a03bbba9a14
- Source dataset
- uspto-grants-2013_07
- Patent number
- US08481550B2
Reaction notes
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