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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1608017Generated: October 30, 2026

2-Methylpropyl 3-carbamoylmethyl-Beta-hydroxy2-(1-methylethyl)-4-oxo-1-imidazolidinebutanoate → N-(2-Amino-2-oxoethyl)-2-(4-hydroxy-2-oxopyrrolidin-1-yl)acetamide

https://huagongshe.com/reaction/1608017

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Methylpropyl 3-carbamoylmethyl-Beta-hydroxy2-(1-methylethyl)-4-oxo-1-imidazolidinebutanoateHCID 14618024—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductN-(2-Amino-2-oxoethyl)-2-(4-hydroxy-2-oxopyrrolidin-1-yl)acetamideHCID 117013040%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of 11.8 g (34.3mol) of 2-methylpropyl 3-carbamoylmethyl-Beta-hydroxy-2-(l-methylethyl)-4-oxo-1-imidazolidinebutanoate in 90 ml of dimethylformamide and 10 ml of water was gently refluxed (external temp. 130° C.) for 24 hours. The solvent was evaporated under reduced pressure. The oily residue was taken up with 40 ml of ethanol and stirred at 0° C. for 30 minutes. The precipitate was collected and crystallized from ethanol/isopropanol 1:1 to give 2.5 g of the title compound as a white powder, m.p. 158°-160° C. Mass spectrum (E.I., 70 eV, 1.5 mA), m/z=197 (M+ --H2O), 180. IR spectrum (oil mull): 3420, 3320, 3220, 1680, 1655 and 1630 cm`31.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04868313
Source datasetuspto-grants-1989_09
ORD IDord-da08c7ac608949e6b0cdbe740efd051b
Source noteuspto-grants-1989_09