HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1291627Generated: November 2, 2026
HCID 19608161, compound → HCID 19607843, compound
https://huagongshe.com/reaction/1291627
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 19608161 | HCID 19608161 | — |
| Reactant | Phthalimide potassium salt | HCID 24194345 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 19607843 | HCID 19607843 | 90.6% |
Reaction Steps
A mixture of 1-{4-[2-(6-bromohexyloxy)benzoylamino]benzoyl}-2,3,4,5-tetrahydro-1H-benzazepine (4.00 g), potassium phthalimide (2.02 g) and dimethylformamide (100 ml) is stirred at 100° C. for 5 hours. The reaction mixture is filtered and the filtrate is distilled off. The resulting residue is extracted with ethyl acetate and the organic layer is washed successively with water and saturated saline solution, and dried over magnesium sulfate. The solvent is distilled off and the resulting residue is purified by silica gel column chromatography (eluent; dichloromethane), and recrystallized from methanol/diethyl ether to give 1-{4-[2-(6-phthalimidohexyloxy)benzoylamino]benzoyl}-2,3,4,5-tetrahydro-1H-benzazepine (4.06 g) as white powder, m.p. 145°-146.5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05753677 |
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| Source dataset | uspto-grants-1998_05 |
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| ORD ID | ord-d5634de3c08049218578cee440fa6481 |
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| Source note | uspto-grants-1998_05 |
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