HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 464170Generated: October 29, 2026
Hydrochloric Acid → HCID 13225503, compound
https://huagongshe.com/reaction/464170
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Acetamidine monohydrochloride | HCID 67170 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | HCID 53970306 | HCID 53970306 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 13225503 | HCID 13225503 | — |
Reaction Steps
In five equal portions 9.0 g (95 mmole) of acetamidine hydrochloride and 22.5 (0.1 mole) of a 4.46M methanol solution of sodium methoxide was added over 3 hr to a solution of 4.5 g (15 mmole) of 1-phenyl-3,4-dihydro-4-[(dimethylamino)methylene]-5H-2-benzazepin-5-one in 180 ml of methanol and 180 ml of methylene chloride. The methylene chloride solution was washed with water, dried over anhydrous sodium sulfate, and concentrated at reduced pressure to give an oil. The oil was dissolved in an excess of 6% methanolic hydrogen chloride and the solvent was removed at reduced pressure to dryness. The residue was crystallized from a mixture of ether and methylene chloride to give a white solid mp 211°-221° C. Recrystallization from a mixture of methanol and ether gave white flakes, mp 217°-227° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04546183 |
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| Source dataset | uspto-grants-1985_10 |
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| ORD ID | ord-59bb213a0aa54c468ab548fddfa38590 |
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| Source note | uspto-grants-1985_10 |
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