Ammonium Hydroxide → HCID 13225509, compound
Reaction equation
[Cl:1][C:2]1[CH:24]=[CH:23][C:5]2[C:6]3[N:22]=[CH:21][N:20]=[CH:19][C:7]=3[CH2:8][N+:9]([O-])=[C:10]([C:11]3[CH:16]=[CH:15][CH:14]=[CH:13][C:12]=3[F:17])[C:4]=2[CH:3]=1.P(Cl)(Cl)Cl.[OH-].[NH4+]>C(Cl)Cl>[Cl:1][C:2]1[CH:24]=[CH:23][C:5]2[C:6]3[N:22]=[CH:21][N:20]=[CH:19][C:7]=3[CH2:8][N:9]=[C:10]([C:11]3[CH:16]=[CH:15][CH:14]=[CH:13][C:12]=3[F:17])[C:4]=2[CH:3]=1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
A mixture of 0.5 g (1.5 mmol) of 9-chloro-7-(2-fluorophenyl)-5H-pyrimido[5,4-d][2]benzazepine-6-oxide, and 1.0 mol (10 mmol) of phosphorous trichloride in 20 ml of methylene chloride was heated at reflux for 2 hr. The mixture was poured over ice, basified with ammonium hydroxide and extracted with methylene chloride. The methylene chloride solution was dried over anhydrous sodium sulfate and concentrated at reduced pressure to dryness. The residue was crystallized from ether to give off-white crystals, mp 122°-124° C.
Workup
- temperaturewas heated
- temperatureat reflux for 2 hr
- additionThe mixture was poured over ice
- extractionextracted with methylene chloride
- dry with materialThe methylene chloride solution was dried over anhydrous sodium sulfate
- concentrationconcentrated at reduced pressure to dryness
- customThe residue was crystallized from ether
- customto give off-white crystals, mp 122°-124° C.
Sources & evidence
- ORD record
- ord-bb8bfeed14f1419cbfc3278142496d00
- Source dataset
- uspto-grants-1984_11
- Patent number
- US04481142
Reaction notes
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