Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2114133Generated: October 31, 2026

HCID 2325055, compound → HCID 69201728, compound

https://huagongshe.com/reaction/2114133

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 2325055HCID 2325055—
Reactant5'-amino-N-(cyclopropylmethyl)-2'-methyl-1,1'-biphenyl-4-carboxamideHCID 11300488—
SolventTetrahydrofuranHCID 8028—
ProductHCID 69201728HCID 6920172836.7%

Reaction Steps

5′-Amino-N-(cyclopropylmethyl)-2′-methyl-1,1′-biphenyl-4-carboxamide (53 mg, 0.189 mmol) and 5-chloro-2-(piperidin-1-yl)pyrimidine-4-carboxylic acid (91.3 mg, 0.38 mmol) were mixed in THF (5 ml) and the mixture shaken in a varian tube for 15 min at room temperature. Carbodiimde resin (500 mg) was added and shaking continued for 48 h. The solution was filtered off and concentrated under vacuum. The residue was chromatographed on a silica gel flash column eluting with ethyl acetate/hexane (1:1) and the solvent evaporated under vacuum to give 5-chloro-N-(4′-{[(cyclopropylmethyl)amino]carbonyl}-6-methyl-1,1′-biphenyl-3-yl)-2-(piperidin-1-yl)pyrimidine-4- carboxamide (35 mg). NMR; δH CDCl3 9.50,(1 H, s), 8.40,(1 H, s), 7.83,(2H, d), 7.64,(1H, dd), 7.56,(1H, d), 7.41,(2H, d), 7.27,(1H, d), 6.24,(1H, t), 3.79,(4H, m), 3.35,(2H, m), 2.22,(3H, s), 1.65,(4H, m), 1.08,(1H, m), 0.82,(2H, m), 0.58,(2H, m), 0.30,(2H, m). LCMS: retention time 3.96 min, MH+504.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07432289B2
Source datasetuspto-grants-2008_10
ORD IDord-02ae794d365f49c9957cdf9468ebf058
Source noteuspto-grants-2008_10