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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2036831Generated: October 25, 2026

Diisopropylethylamine → 3-(1-Cyanocyclopropanecarboxamido)biphenyl-2-carboxamide

https://huagongshe.com/reaction/2036831

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant1-Cyanocyclopropanecarboxylic acidHCID 2733259—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
ReactantHCID 66965572HCID 66965572—
SolventDichloromethaneHCID 6344—
Product3-(1-Cyanocyclopropanecarboxamido)biphenyl-2-carboxamideHCID 6705588974%

Reaction Steps

To a solution of 1-cyanocyclopropanecarboxylic acid (0.75 g, 7 mmol) in DCM (40 mL) was added HATU (3.5 g, 10 mmol) and DIPEA (3.4 mL, 20 mmol). After stirring at room temperature for 1 h, 3-aminobiphenyl-2-carboxamide (from example 218: 1 g, 5 mmol) was added and the reaction mixture stirred for an additional 16 h. The reaction mixture was washed with water and the organic phase dried, filtered, concentrated under reduced pressure and purified by silica gel chromatography (60% ethyl acetate in hexanes) to provide 3-(1-cyanocyclopropanecarboxamido)biphenyl-2-carboxamide (0.75 g, 74% yield) as a white solid. LCMS Method T: retention time 1.53 min; [M+1]=306.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08575184B2
Source datasetuspto-grants-2013_11
ORD IDord-8627cf1220c5435daa228f61f03c2100
Source noteuspto-grants-2013_11