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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2114139Generated: November 1, 2026

2-cyclopropylquinoline-4-carboxylic acid → HCID 69203211, compound

https://huagongshe.com/reaction/2114139

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-cyclopropylquinoline-4-carboxylic acidHCID 275785—
Reactant5'-amino-N-(cyclopropylmethyl)-2'-methyl-1,1'-biphenyl-4-carboxamideHCID 11300488—
SolventTetrahydrofuranHCID 8028—
ProductHCID 69203211HCID 69203211—

Reaction Steps

5′-Amino-N-(cyclopropylmethyl)-2′-methyl-1,1′-biphenyl-4-carboxamide (42 mg, 0.15 mmol) and 2-cyclopropylquinoline-4-carboxylic acid (85.3 mg, 0.4 mmol) were mixed in THF (5 ml) and the mixture shaken in a varian tube for 30 min at room temperature. Carbodiimde resin (442 mg, 0.5 mmol) was added and shaking continued for 18 h. The solution was filtered off, the resin washed with THF and methanol and the combined filtrate and washings reduced to dryness under vacuum. The residue was dissolved in ethyl acetate, washed with hydrochloric acid (1M) and aqueous sodium hydrogen carbonate. The solvent was evaporated from the organic fraction under vacuum to give 2-cyclopropyl-N-(4′-{[(cyclopropylmethyl)amino]carbonyl}-6-methyl-1,1′-biphenyl-3-yl)quinoline-4-carboxamide. NMR; δH [2H6]—DMSO 10.74,(1H, s), 8.62,(1H, t), 8.04,(1H, d), 7.94-7.90,(3H, m), 7.74-7.70,(3H, m), 7.62,(1H, s), 7.53,(1H, m), 7.45,(2H, d), 7.33,(1H, d), 3.16,(2H, t), 2.37,(1H, m), 2.22,(3H, s), 1.15-1.10,(5H, m), 0.43,(2H, m), 0.24,(2H, m). LCMS: retention time 3.61 min, MH+476.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07432289B2
Source datasetuspto-grants-2008_10
ORD IDord-acb732e531f64193a31cce529605ccf9
Source noteuspto-grants-2008_10