Hydrochloric Acid → Methylpyrrolo[3,2,1-kl]phenoxazine-1-one-2-carboxylate
Reaction equation
[H-].[Na+].[CH:3]1[N:17]2[C:18]3[C:9]([O:10][C:11]4[CH:12]=[CH:13][CH:14]=[CH:15][C:16]=42)=[CH:8][CH:7]=[CH:6][C:5]=3[CH:4]=1.Cl[C:20]([O:22][CH3:23])=[O:21].Cl.CN(C)C=[O:28]>>[CH3:23][O:22][C:20]([CH:4]1[C:5]2[CH:6]=[CH:7][CH:8]=[C:9]3[O:10][C:11]4[CH:12]=[CH:13][CH:14]=[CH:15][C:16]=4[N:17]([C:18]=23)[C:3]1=[O:28])=[O:21]Participants
Procedure
To a slurry of sodium hydride (0.39 g) in 20 ml of DMF (dimethylformamide) was added pyrrolo[3,2,1-kl]phenoxazine (1.4 g), prepared as described according to Preparation 2, and the resulting dark red solution was stirred at room temperature for 0.5 hours. To this solution, was added methyl chloroformate (0.95 g), dropwise, over a period of 10 minutes. The reaction mixture was stirred for 2 hours at room temperature, and it was then poured onto ice water (200 ml). The resulting mixture was then acidified to pH 2.0 with concentrated HCl and the mixture was then extracted with methylene chloride (200 ml). The extract was washed with water, dried and evaporated to dryness to yield the title compound as a solid (0.06 g; m.p. 124°-127° C.).
Workup
- customprepared
- customas described according to Preparation 2
- waitdropwise, over a period of 10 minutes
- stirringThe reaction mixture was stirred for 2 hours at room temperature
- additionit was then poured onto ice water (200 ml)
- extractionthe mixture was then extracted with methylene chloride (200 ml)
- washThe extract was washed with water
- customdried
- customevaporated to dryness
Sources & evidence
- ORD record
- ord-31377a35c8b047ab9c7d2e2811e7ae32
- Source dataset
- uspto-grants-1997_04
- Patent number
- US05624929
Reaction notes
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