HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 964982Generated: October 30, 2026
Hydrochloric Acid → HCID 22444742, compound
https://huagongshe.com/reaction/964982
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ammonium Carbonate | HCID 517111 | — |
| Reactant | HCID 22444726 | HCID 22444726 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 22444742 | HCID 22444742 | — |
Reaction Steps
550 mg of methyl 4 -[4 -(4 -cyanophenyl)-1-piperazinyl]-1-ethoxycarbonylmethyl-3-piperidinepropionate was dissolved in 20 ml of ethanol, into which hydrogen chloride was made to blow at from -10° C. to -20° C. until saturation. This was heated up to room temperature and stirred overnight, and thereafter the solvent was. removed by distillation. The residue thus obtained was dissolved in 20 ml of ethanol, and 1.0 g of ammonium carbonate was added thereto and stirred at room temperature overnight. The solvent was removed from the reaction mixture by distillation, and the resulting residue was purified by silica gel column chromatography (using an eluent of chloroform/methanol=10/1) to obtain 500 mg of ethyl 4-[4-(4-amidinophenyl)-1-piperazinyl]-1-ethoxycarbonylmethyl-3-piperidinepropionate hydrochloride.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05773442 |
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| Source dataset | uspto-grants-1998_06 |
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| ORD ID | ord-08970ba4ab944292a6786c5a05be016c |
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| Source note | uspto-grants-1998_06 |
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