Hydrochloric Acid → HCID 14347194, compound
Reaction equation
[N:1]1[CH:6]=[CH:5][C:4]([C:7]2[CH:12]=[CH:11][N:10]=[C:9]([NH:13][C:14]3[CH:19]=[CH:18][C:17]([NH:20]C(=O)C)=[CH:16][CH:15]=3)[N:8]=2)=[CH:3][CH:2]=1.[ClH:24]>O>[ClH:24].[N:1]1[CH:2]=[CH:3][C:4]([C:7]2[CH:12]=[CH:11][N:10]=[C:9]([NH:13][C:14]3[CH:19]=[CH:18][C:17]([NH2:20])=[CH:16][CH:15]=3)[N:8]=2)=[CH:5][CH:6]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A 2.85 g amount of N-[4-[[4-(4-pyridinyl)-2-pyrimidinyl]amino]phenyl]acetamide was added to a mixture of 10 ml of concentrated hydrochloric acid and 10 ml of water. The reaction mixture was heated at reflux for 90 minutes, then evaporated in vacuo to obtain a solid. The solid was recrystallized from 3A ethanol/water and gave 2.31 g of the desired product as a yellow crystalline solid, mp 292°-295° C.
Workup
- temperatureThe reaction mixture was heated
- temperatureat reflux for 90 minutes
- customevaporated in vacuo
- customto obtain a solid
- customThe solid was recrystallized from 3A ethanol/water
Sources & evidence
- ORD record
- ord-4b996f85afd147f0a15fc49e8b4f0cbb
- Source dataset
- uspto-grants-1989_10
- Patent number
- US04876252
Reaction notes
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