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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 347656Generated: October 30, 2026

Dimethylamine, hydrochloride → L-trans4Hydroxyproline N,N-dimethylamide hydrochloride

https://huagongshe.com/reaction/347656

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylamine, hydrochlorideHCID 10473—
ReactantDiisopropylethylamineHCID 81531—
Reactant(2S,4R)-4-hydroxy-1-[(2-methylpropan-2-yl)oxycarbonyl]pyrrolidine-2-carboxylic acidHCID 88804—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
Solvent1,4-Dioxane hydrochlorideHCID 20443148—
ProductL-trans4Hydroxyproline N,N-dimethylamide hydrochlorideHCID 131725849—

Reaction Steps

To a solution of BOC-hydroxyproline (2.99 g, 13.89 mmol) in dichloromethane (100 ml) were added N,N-diisopropylethylamine (3.7 ml, 21.24 mmol), 4-(dimethylamino)pyridine (1.74 g, 14.24 mmol), dimethylamine hydrochloride (1.72 g, 21.09 mmol) and WSCDI (3.17 g, 16.68 mmol). The mixture was stirred at room temperature for 30 h. The mixture was diluted with dichloromethane (100 ml) and washed with 0.3M KHSO4, saturated sodium bicarbonate solution and brine, dried over MgSO4, and concentrated in vacuo to give a colourless gum. This crude material was taken up in 4N HCl/dioxan (50 ml) and stirred at room temperature for 1 hr and then concentrat d in vacuo. The residue was azeotroped with toluene and diethyl ether to give a white solid; yield 0.45 g (17%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07176195B2
Source datasetuspto-grants-2007_02
ORD IDord-c93dfe279f6944dea78b7807fc08f14e
Source noteuspto-grants-2007_02