Dichloromethane → HCID 178482910, compound
Reaction equation
[CH3:1][N:2]([CH3:31])[C:3]1[CH:4]=[C:5]([F:30])[C:6]2[N:7](C(OC(C)(C)C)=O)[C:8]3[C:13]([S:14][C:15]=2[CH:16]=1)=[CH:12][C:11]([N:17]1[CH2:22][CH2:21][O:20][CH2:19][CH2:18]1)=[CH:10][CH:9]=3.[Cl:32]CCl>>[Cl-:32].[CH3:1][N:2]([CH3:31])[C:3]1[CH:4]=[C:5]([F:30])[C:6]2[C:15]([CH:16]=1)=[S+:14][C:13]1[C:8](=[CH:9][CH:10]=[C:11]([N:17]3[CH2:22][CH2:21][O:20][CH2:19][CH2:18]3)[CH:12]=1)[N:7]=2Participants
3
Conditions
- Temperature
- 40 °C
Procedure
To a solution 3-dimethylamino-7-morpholino-1-fluoro-10-Boc-phenothiazine (15) (100 mg) in dichloromethane (10 mL) HCl (1 mL, 4 M solution in 1,4-dioxane)) was added. The reaction mixture was stirred at 40° C. for 3 h. Solvent was removed under vacuum. Product was purified by flash chromatography.
Workup
- customSolvent was removed under vacuum
- customProduct was purified by flash chromatography
Sources & evidence
- ORD record
- ord-e9bdc129581e4f1189be83baf8ed3d7a
- Source dataset
- uspto-grants-2014_09
- Patent number
- US08828986B2
Reaction notes
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