Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1091277Generated: November 1, 2026

Sodium hydride → HCID 58691259, compound

https://huagongshe.com/reaction/1091277

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantMethyl bromoacetateHCID 60984—
ReactantHCID 58691278HCID 58691278—
SolventDimethylformamideHCID 6228—
ProductHCID 58691259HCID 5869125996.9%

Reaction Steps

61 mg (2.54 mmol) of sodium hydride are added to the solution of 1 g (2.31 mmol) of tert-butyl (2R,4R)-4-methoxy-2-[4-(3-oxomorpholin-4-yl)-phenylcarbamoyl]pyrrolidine-1-carboxylate (prepared analogously to Example 7.1) in 20 ml of dimethylformamide, and the mixture is stirred at room temperature for 30 minutes. 022 mg (2.31 mmol) of methyl bromoacetate is subsequently added to the reaction mixture, which is then left to stir at room temperature for 12 hours. The reaction mixture is then evaporated under reduced pressure, the residue is taken up in 20 ml of water, and the aqueous solution is extracted three times with 20 ml of methylene chloride each time. Drying of the combined organic phases over sodium sulfate and stripping-off of the solvent gives 1.1 g of tert-butyl (2R,4R)-4-methoxy-2-{methoxycarbonylmethyl-[4-(3-oxomorpholin-4-yl)phenyl]-carbamoyl}pyrrolidine-1-carboxylate as a yellow oil; ESI (M-BOC) 392.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08129373B2
Source datasetuspto-grants-2012_03
ORD IDord-99ac2b5024ae4142b8c97f54542da1b8
Source noteuspto-grants-2012_03