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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2114115Generated: October 30, 2026

5-(Pyridin-2-yl)thiophene-2-carboxylic acid → HCID 69202963, compound

https://huagongshe.com/reaction/2114115

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-(Pyridin-2-yl)thiophene-2-carboxylic acidHCID 736482—
Reactant5'-amino-N-(cyclopropylmethyl)-2'-methyl-1,1'-biphenyl-4-carboxamideHCID 11300488—
ProductHCID 69202963HCID 69202963—

Reaction Steps

N-(4′-{[(Cyclopropylmethyl)amino]carbonyl}-6-methyl-1,1′-biphenyl-3-yl)-5-(pyrid-2-yl)thiophene-2- carboxamide was prepared from 5′-amino-N-(cyclopropylmethyl)-2′-methyl-1,1′-biphenyl-4-carboxamide and 5-(pyrid-2-yl)thiophene-2-carboxylic acid using method D. The product was further purified by preparative HPLC. NMR; δH [2H6]—DMSO 10.29,(1H, s), 8.63,(1H, t), 8.58,(1H, d), 8.02-7.99,(2H, m), 7.94,(2H, d), 7.90-7.86,(2H, m), 7.70,(1H, dd), 7.65,(1H, d), 7.46,(2H, d), 7.35,(1H, m), 7.30,(1H, d), 3.17,(2H, t), 2.21,(3H, s), 1.04,(1H, m), 0.43,(2H, m), 0.24,(2H, m). LCMS: retention time 3.60 min, MH+468.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07432289B2
Source datasetuspto-grants-2008_10
ORD IDord-ecd4377d668643a1b479bdcb6fc78559
Source noteuspto-grants-2008_10