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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1735413Generated: October 30, 2026

Hydrochloric Acid → (S)-2-[[(S)-2-(4-Hydroxy-1-oxobutyl)-1-pyrrolidinyl]carbonyl]-N-(phenylmethyl)-1-pyrrolidinecarboxamide

https://huagongshe.com/reaction/1735413

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantBenzyl isocyanateHCID 76639—
ReactantL-ProlineHCID 145742—
Reactant(S)-1-(tert-Butoxycarbonyl)-2-[1-hydroxy-4-(phenylmethyloxy)butyl]pyrrolidineHCID 67745428—
SolventDimethylformamideHCID 6228—
SolventTriethylamineHCID 8471—
Product(S)-2-[[(S)-2-(4-Hydroxy-1-oxobutyl)-1-pyrrolidinyl]carbonyl]-N-(phenylmethyl)-1-pyrrolidinecarboxamideHCID 5437394777.9%

Reaction Steps

4N Hydrochloric acid (1,4-dioxane solution, 20 ml) was added to (S)-1-(tert-butoxycarbonyl)-2-[1-hydroxy-4(phenylmethyloxy)butyl]pyrrolidine (high polar isomer, 3.00 g) and the mixture was allowed to stand at room temperature for 30 minutes. The reaction mixture was concentrated and the residue was reacted with N-(benzylamincarbonyl)-L-proline obtained by stirring L-proline (0.99 g), benzyl isocyanate (0.97 g) and triethylamine (0.87 g) in DMF (10 ml) at room temperature for 1 hour, in the same manner as in Example 5-b), to give the title compound (2.20 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05536737
Source datasetuspto-grants-1996_07
ORD IDord-1ad2442966b24a8d9d95dcbb32e1e2eb
Source noteuspto-grants-1996_07