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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1474146Generated: 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/1474146

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 numberUS09018206B2
Source datasetuspto-grants-2015_04
ORD IDord-ac4b7085d96341119bc82b61e5053fb6
Source noteuspto-grants-2015_04