HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1440694Generated: October 30, 2026
Triethylamine → Ethyl cis-[4-(4-amino-5-chloro-2-methoxybenzamido)-3-methoxypiperidino]formate
https://huagongshe.com/reaction/1440694
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Reactant | Ethyl cis-(4-amino-3-methoxypiperidino)formate | HCID 13677746 | — |
| Reactant | 4-Amino-3-chloro-5-methoxybenzoic acid | HCID 15164586 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Ethyl cis-[4-(4-amino-5-chloro-2-methoxybenzamido)-3-methoxypiperidino]formate | HCID 11132816 | — |
Reaction Steps
To a mixture of 33.3 g of 4-amino-5-chloro-3-methoxybenzoic acid, 27.0 ml of triethylamine, and 450 ml of tetrahydrofuran, 16.2 ml of ethyl chloroformate was added dropwise with stirring under ice-cooling. Stirring was continued for 1.5 hours under ice-cooling, a solution of 35.0 g of ethyl cis-(4-amino-3-methoxypiperidino)formate in 50 ml of tetrahydrofuran was added dropwise. After being stirred for 20 hours at room temperature, the reaction mixture was concentrated under reduced pressure. Water was added to the residue, and the mixture was extracted with dichloromethane. The extract was washed with aqueous potassium carbonate solution, dried over anhydrous sodium sulfate, and then concentrated under reduced pressure. The residue was washed with diethyl ether to give 44.5 g of colorless crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05500422 |
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| Source dataset | uspto-grants-1996_03 |
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| ORD ID | ord-8b16be34c60b45eeb20d8cb0bdfcf621 |
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| Source note | uspto-grants-1996_03 |
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