HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 847393Generated: October 31, 2026
Hydroxyamine hydrochloride → HCID 86746098, compound
https://huagongshe.com/reaction/847393
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydroxyamine hydrochloride | HCID 443297 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 67755601 | HCID 67755601 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 86746098 | HCID 86746098 | 101.3% |
Reaction Steps
To a suspension of 6.0 g of 2-acetyl-5,6,7,8-tetrahydro-5-[4-(4-(2-pyrimidinyl)-1-piperazinyl)butyl]-4H-thieno[3,2-c]azepin-4-one maleate in 100 ml of ethanol were added 0.92 g of hydroxyamine hydrochloride and 4.0 g of sodium hydrogencarbonate with stirring and the mixture was refluxed for 5 hours. After cooling, the mixture was concentrated under reduced pressure, to the residue was added water and the solution was extracted with chloroform. The extract was washed with water, dried and concentrated in vacuo. The resulting crystals were recrystallized from a mixed solvent of ethanol and isopropyl ether to give 4.95 g of 5,6,7,8-tetrahydro-2-(1-(hydroxyimino)ethyl)-5-[4-(4-(2-pyrimidinyl)-1-piperazinyl)butyl]-4H-thieno[3,2-c]azepin-4-one as white crystals, melting at 144°-146° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05141930 |
|---|
| Source dataset | uspto-grants-1992_08 |
|---|
| ORD ID | ord-390a9a693fa44756a249b210a9bc3480 |
|---|
| Source note | uspto-grants-1992_08 |
|---|