Nicotinoyl chloride → HCID 20548751, compound
Reaction equation
[ClH:1].Cl.[CH2:3]([C:9]1[NH:10][NH:11][C:12]2[N:18]=[CH:17][CH:16]=[CH:15][C:13]=2[N:14]=1)[CH2:4][CH2:5][CH2:6][CH2:7][CH3:8].[C:19]([Cl:27])(=[O:26])[C:20]1[CH:25]=[CH:24][CH:23]=[N:22][CH:21]=1>>[ClH:27].[ClH:1].[CH2:3]([C:9]1[NH:10][N:11]([C:19](=[O:26])[C:20]2[CH:25]=[CH:24][CH:23]=[N:22][CH:21]=2)[C:12]2[N:18]=[CH:17][CH:16]=[CH:15][C:13]=2[N:14]=1)[CH2:4][CH2:5][CH2:6][CH2:7][CH3:8]Participants
3
Procedure
12 g (0.04 mole) of 3-n-hexyl-1,2-dihydropyrido-[3,2-e]-as-triazine dihydrochloride are boiled with an excess of nicotinic chloride. The reaction mixture is cooled and the separated product is filtered off.
Workup
- temperatureThe reaction mixture is cooled
- filtrationthe separated product is filtered off
Sources & evidence
- ORD record
- ord-a4b8a856920741d6aeb13e11fbc5efc4
- Source dataset
- uspto-grants-1982_03
- Patent number
- US04320127
Reaction notes
Loading…