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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 425406Generated: October 30, 2026

4-Methylmorpholine → HCID 66705859, compound

https://huagongshe.com/reaction/425406

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylmorpholineHCID 7972—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
ReactantBoc-(R)-alpha-(4-bromobenzyl)prolineHCID 2761850—
ReactantHCID 55289824HCID 55289824—
ReactantHCID 178418300HCID 178418300—
SolventDichloromethaneHCID 6344—
ProductHCID 66705859HCID 66705859—

Reaction Steps

N-methylmorpholine (6.4 mL, 58.6 mmol) was added to an ambient temperature solution of 2-(4-bromobenzyl)-1-(tert-butoxycarbonyl)proline (5.0 g, 13 mmol), 1-amino-4,4-dimethylhexan-2-ol (1.89 g, 13 mmol), 1-[3-(dimethylamino) propyl]-3-ethylcarbodiimide hydrochloride (3.0 g, 15.6 mmol), and hydroxybenzotriazole (2.1 g, 15.6 mmol) in dichloromethane (51 mL). After stirring at ambient temperature overnight, the reaction mixture was quenched with water. The organic phase was dried (magnesium sulfate), filtered, and concentrated in vacuo to afford tert-butyl 2-(4-bromobenzyl)-2-{[(2-hydroxy-4,4-dimethylhexyl)amino]carbonyl}pyrrolidine-1-carboxylate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08106070B2
Source datasetuspto-grants-2012_01
ORD IDord-de5aeec9be574ddc8fdeb2a07ed892c0
Source noteuspto-grants-2012_01