Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 537848Generated: October 29, 2026

Cyclopropylamine → HCID 67975549, compound

https://huagongshe.com/reaction/537848

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclopropylamineHCID 69828—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 67975407HCID 67975407—
Reactant2-(1H-7-Azabenzotriazol-1-yl)-1,1,3,3-tetramethyl uronium hexafluorophosphate MethanaminiumHCID 86621144—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 67975549HCID 6797554926.5%

Reaction Steps

In a 100 ml dry flask, (3-{[5-chloro-1-(4-fluorobutyl)-1H-benzimidazol-2-yl]methyl}-2-oxo-2,3-dihydro-1H-imidazo[4,5-c]pyridin-1-yl)acetic acid (P67, 300 mg, 0.69 mmol), diisopropylethylamine (0.29 mL, 2.08 mmol, 3 eq.), cyclopropylamine (60 μL, 0.83 mmol, 1.2 eq.) and 2-(1H-7-Azabenzotriazol-1-yl)-1,1,3,3-tetramethyl uronium hexafluorophosphate Methanaminium (HATU, 316.9 mg, 0.83 mmol, 1.2 eq.) were dissolved in DMF (50 mL). The solution was placed under N2 atmosphere and stirred at room temperature during 1 hour. The reaction mixture was diluted with water (20 ml) and extracted with dichloromethane (50 mL). The organic layer was dried with MgSO4 and evaporated. The residue was further crystallized in diisopropylether/acetonirile. The solid was filtered off and dried into the oven for 16 hours which gave 2-(3-{[5-chloro-1-(4-fluorobutyl)-1H-benzimidazol-2-yl]methyl}-2-oxo-2,3-dihydro-1H-imidazo[4,5-c]pyridin-1-yl)-N-cyclopropylacetamide (P68, 86 mg, 26%) as a white solid; LCMS m/z=471 (M+H)+

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08865705B2
Source datasetuspto-grants-2014_10
ORD IDord-542ffc1e64ec4852a182fe25a9e2443a
Source noteuspto-grants-2014_10