Methanol → HCID 13853731, compound
Reaction equation
[CH3:1][O:2][C:3]1[C:16]2[C:7]([S:8][C:9]3[C:14]([N:15]=2)=[CH:13][CH:12]=[C:11]([O:17][CH3:18])[CH:10]=3)=[CH:6][C:5](=[O:19])[CH:4]=1.[Br:20]Br.CO>C(O)(=O)C>[Br:20][C:6]1[C:5](=[O:19])[CH:4]=[C:3]([O:2][CH3:1])[C:16]2[C:7]=1[S:8][C:9]1[C:14](=[CH:13][CH:12]=[C:11]([O:17][CH3:18])[CH:10]=1)[N:15]=2Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
To a suspension of 1,7-dimethoxy-3H-phenothiazin-3-one (300 mg) in acetic acid (9 ml) was added a 0.63M solution of Br2 in acetic acid (1.92 ml). After 15 minutes, methanol was added and the solid filtered, washed with ether and air dried to afford the title compound (353 mg), m.p. 267°-270° C. (dec).
Workup
- filtrationthe solid filtered
- washwashed with ether and air
- customdried
Sources & evidence
- ORD record
- ord-933d288bd42b4593a7a4458eb5a2bf74
- Source dataset
- uspto-grants-1987_05
- Patent number
- US04667032
Reaction notes
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