HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1250528Generated: October 25, 2026
Hydrochloric Acid → 4-amino-5-chloro-2-methoxy-N-(piperidin-4-ylmethyl)benzamide
https://huagongshe.com/reaction/1250528
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | N-tert-butyloxycarbonyl-4-(4-amino-5-chloro-2-methoxyphenylcarbonylaminomethyl)piperidine | HCID 11200348 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 4-amino-5-chloro-2-methoxy-N-(piperidin-4-ylmethyl)benzamide | HCID 9817713 | — |
Reaction Steps
To a solution of N-tert-butyloxycarbonyl-4-(4-amino-5-chloro-2-methoxyphenylcarbonylaminomethyl)piperidine (500 mg, 1.26 mmol) in methanol solution (30 ml) was added an ethereal 1N hydrogen chloride solution (12.6 ml, 12.6 mmol). The solution was heated at 50° C. The reaction mixture became heterogeneous within 5 min. After 1.5 h, the reaction mixture was concentrated to give a white solid which was suspended in diethylether and filtered to give 4-(4-amino-5-chloro-2-methoxyphenylcarbonylamino-methyl)piperidine as a bis-hydrochloride salt (433 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06339087B1 |
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| Source dataset | uspto-grants-2002_01 |
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| ORD ID | ord-8bb0010645d6410288b5b7f8f176b428 |
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| Source note | uspto-grants-2002_01 |
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