HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 464538Generated: October 30, 2026
Ammonium Hydroxide → HCID 13225521, compound
https://huagongshe.com/reaction/464538
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | 1-Methylpiperazine | HCID 53167 | — |
| Reactant | HCID 13225515 | HCID 13225515 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 13225521 | HCID 13225521 | — |
Reaction Steps
To a solution of 3.0 g (0.00838 mol) of 2,9-dichloro-7-(2-fluorophenyl)-5H-pyrimido[5,4-d][2]benzazepine in 8 ml of N,N-dimethylformamide was added 2 g (0.02 mol) of N-methylpiperazine. After 20 hr ice water (40 ml) was added to the reaction which was then filtered. The solid was partitioned between 50 ml of dichloromethane and 50 ml of 1N hydrochloride acid, and the pH was adjusted to 1-2 with ammonium hydroxide. The resulting precipitate was filtered and recrystallized twice from methanol to give white prisms, mp 187°-194° C. The acid layer was made basic with ammonium hydroxide, and extracted with 100 ml of dichloromethane which was dried and evaporated. The oil was acidified with 1N hydrochloric acid, adjusted to pH 1-2 with ammonium hydroxide, cooled and filtered. The precipitate was recrystallized from methanol to give a further crop of the product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04547581 |
|---|
| Source dataset | uspto-grants-1985_10 |
|---|
| ORD ID | ord-7af6cbf5486045828b5a4676a3d14220 |
|---|
| Source note | uspto-grants-1985_10 |
|---|