HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2382365Generated: November 1, 2026
(R)-(+)-1-Boc-3-aminopyrrolidine → HCID 66630665, compound
https://huagongshe.com/reaction/2382365
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | (R)-(+)-1-Boc-3-aminopyrrolidine | HCID 854070 | — |
| Reactant | Isonicotinoyl chloride hydrochloride | HCID 12262826 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 66630665 | HCID 66630665 | — |
Reaction Steps
A cooled (0° C.) stirred solution of (R)-3-amino-pyrrolidine-1-carboxylic acid tert-butyl ester (1.0 g, 5.36 mmol) and TEA (1.5 ml, 11.0 mmol) in THF (10 ml) is treated dropwise over 1 minute with pyridine-4 carbonyl chloride hydrochloride (0.935 g, 5.25 mmol). After 5 minutes, the reaction mixture is allowed to warm to room temperature and stirred overnight. The resulting mixture is diluted with EtOAc and washed twice with saturated sodium bicarbonate solution followed by brine. The organic portion is dried (MgSO4) and concentrated in vacuo. The crude product is purified by recrystallisation from EtOAc/iso-hexane to afford the title product. [MH+ 292].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08258141B2 |
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| Source dataset | uspto-grants-2012_09 |
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| ORD ID | ord-39533bc3628d43e783e4b8be28f7f157 |
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| Source note | uspto-grants-2012_09 |
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