HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1489094Generated: October 31, 2026
HCID 22903525, compound → HCID 22903473, compound
https://huagongshe.com/reaction/1489094
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 22903525 | HCID 22903525 | — |
| Reactant | Phthalimide potassium salt | HCID 24194345 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 22903473 | HCID 22903473 | 103.1% |
Reaction Steps
To a solution of 7-chloro-5-(2-methanesulfonyloxyethyl)-1-[6-(2-chlorobenzoylamino)nicotinoyl]-2,3,4,5-tetrahydro-1H-benzazepine (1.6 g) in dimethylformamide (30 ml) is added potassium phthalimide (0.58 g), and the mixture is stirred at 110° C. for 3 hours. The mixture is poured into ice-water, and the mixture is extracted with dichloromethane. The extract is washed with water, dried over magnesium sulfate, and evaporated under reduced pressure to remove the solvent. The residue is purified by silica gel column chromatography to give 7-chloro-5-(2-phthalimidoethyl)-1-[6-(2-chlorobenzoylamino)nicotinoyl]-2,3,4,5-tetrahydro-1H-benzazepine (1.8 g) as colorless amorphous.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05677299 |
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| Source dataset | uspto-grants-1997_10 |
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| ORD ID | ord-ed9e54eba54c447784a9ce55d2ecfabd |
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| Source note | uspto-grants-1997_10 |
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