Ammonium Hydroxide → HCID 13225509, compound

HRID 1979592Notes

Reaction equation

HRID 1979592 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]=1

Participants

5

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

  1. temperaturewas heated
  2. temperatureat reflux for 2 hr
  3. additionThe mixture was poured over ice
  4. extractionextracted with methylene chloride
  5. dry with materialThe methylene chloride solution was dried over anhydrous sodium sulfate
  6. concentrationconcentrated at reduced pressure to dryness
  7. customThe residue was crystallized from ether
  8. 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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