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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 882854Generated: November 2, 2026

Diisopropylethylamine → (2R)-N-(4-(Cyclopropylamino)-3-hydroxy-4-oxo-1-phenylbutan-2-yl)-1-(2-methoxy-6-(trifluoromethyl)benzyl)-5-oxopyrrolidine-2-carboxamide

https://huagongshe.com/reaction/882854

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
Reactant(R)-1-(2-methoxy-6-(trifluoromethyl)benzyl)-5-oxopyrrolidine-2-carboxylic acidHCID 66644853—
Reactant3-Amino-N-cyclopropyl-2-hydroxy-4-phenylbutanamide HydrochlorideHCID 66645025—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product(2R)-N-(4-(Cyclopropylamino)-3-hydroxy-4-oxo-1-phenylbutan-2-yl)-1-(2-methoxy-6-(trifluoromethyl)benzyl)-5-oxopyrrolidine-2-carboxamideHCID 67095048126.1%

Reaction Steps

DIPEA (0.8 ml, 4.58 mmol) was added to a mixture of (R)-1-(2-methoxy-6-(trifluoromethyl)benzyl)-5-oxopyrrolidine-2-carboxylic acid (234 mg, 0.74 mmol) and 3-amino-N-cyclopropyl-2-hydroxy-4-phenylbutanamide hydrochloride (200 mg, 0.74 mmol) in DCM (50 mL). After stirring for 10 min HATU (337 mg, 0.89 mmol) was added and the stirring was continued overnight. The reaction mixture was diluted with DCM and water was added. The organic layer was separated and the aqueous layer was extracted with DCM. The combined organic layers were washed with saturated aqueous NaHCO3 solution, saturated aqueous NaCl solution and dried over MgSO4. Removal of the solvent in vacuo provided the title compound (498 mg, 95%, ca. 75% purity).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08236798B2
Source datasetuspto-grants-2012_08
ORD IDord-9a970da748ed42618b6118cf4e874e8c
Source noteuspto-grants-2012_08