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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2114138Generated: October 30, 2026

HCID 275791, compound → HCID 69203895, compound

https://huagongshe.com/reaction/2114138

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 275791HCID 275791—
Reactant5'-amino-N-(cyclopropylmethyl)-2'-methyl-1,1'-biphenyl-4-carboxamideHCID 11300488—
SolventTetrahydrofuranHCID 8028—
ProductHCID 69203895HCID 69203895—

Reaction Steps

5′-Amino-N-(cyclopropylmethyl)-2′-methyl-1,1′-biphenyl-4-carboxamide (42 mg, 0.15 mmol) and 2-cyclohexyl-6-methylquinoline-4-carboxylic acid (107.7 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-cyclohexyl-N-(4′-{[(cyclopropylmethyl)amino]carbonyl}-6-methyl-1,1′-biphenyl-3-yl)-6-methylquinoline-4-carboxamide. NMR; δH [2H6]—DMSO 10.69,(1H, s), 8.62,(1H, t), 7.95-7.90,(3H, m), 7.82,(1H, s), 7.70,(2H, m), 7.60,(1H, dd, 7.56, (1H, s), 7.46,(2H, d), 7.33,(1H, d), 3.16,(2H, t), 2.90,(1H, m), 2.47,(3H, s), 2.22,(3H, s), 1.95,(2H, m), 1.84,(2H, m), 1.74-1.61,(3H, m), .46-1.26,(3H, m), 1.04,(1H, m), 0.43,(2H, m), 0.24,(2H, m). LCMS: retention time 3.93 min, MH+532.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07432289B2
Source datasetuspto-grants-2008_10
ORD IDord-a6fb3c530cda4933964fda63d6762a74
Source noteuspto-grants-2008_10