Acetyl chloride → HCID 12909300, compound
Reaction equation
[NH2:1][C:2]1[CH:3]=[CH:4][C:5]2[O:10][CH2:9][C:8]3=[N:11][C:12]([C:14]([O:16][CH3:17])=[O:15])=[CH:13][N:7]3[C:6]=2[CH:18]=1.[C:19](Cl)(=[O:21])[CH3:20]>CN(C)C=O>[C:19]([NH:1][C:2]1[CH:3]=[CH:4][C:5]2[O:10][CH2:9][C:8]3=[N:11][C:12]([C:14]([O:16][CH3:17])=[O:15])=[CH:13][N:7]3[C:6]=2[CH:18]=1)(=[O:21])[CH3:20]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
By the procedure of Step C in Example 1, methyl 8-amino-4H-imidazo[2,1-c][1,4]-benzoxazine-2-carboxylate and acetyl chloride were reacted in dimethylformamide as solvent to obtain a 72% yield of methyl 8-acetamido-4H-imidazo-[2,1-c][1,4]-benzoxazine-2-carboxylate with a melting point of 216-9° C.
Sources & evidence
- ORD record
- ord-e2c29dd5f5be4a5285dddd60dcbcae33
- Source dataset
- uspto-grants-1979_03
- Patent number
- US04145419
Reaction notes
Loading…