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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 29273Generated: October 29, 2026

HCID 68713207, compound → HCID 11419551, compound

https://huagongshe.com/reaction/29273

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 68713207HCID 68713207—
SolventDichloromethaneHCID 6344—
SolventTrifluoroacetic acidHCID 6422—
ProductHCID 11419551HCID 1141955173.1%

Reaction Steps

N-({4′-[(1-benzofuran-2-ylcarbonyl)amino]-1,1′-biphenyl-4-yl}sulfonyl)-L-valine t-butyl ester (60 mg) was dissolved in a 95% solution of TFA in methylene chloride (5 mL). The solution was stirred at room temperature for 4 h and the solvent was removed under vacuum. The crude product was triturated with hexane/ethyl acetate (95:5) three times. The product was lyophilized with benzene to give 36 mg of N-({4′-[(1-benzofuran-2-ylcarbonyl)amino]-1,1′-biphenyl-4-yl}sulfonyl)glycine. LCMS MH+ (m/z) 493. 1H NMR (300 MHz, DMSO-d6): δ 10.53 ppm (s, 1H), 7.81-7.54 ppm (m, 11H), 7.34 ppm (dd, 1H, J1=8.4 Hz, J2=8.4 Hz), 7.20 ppm (dd, 1H, J1=8.4 Hz, J2=8.4 Hz), 3.35 ppm (d, 1H J=6.0 Hz), 1.79 ppm (m, 1H), 0.63 ppm (dd, 6H, J1=13.8 Hz, J2=6.6 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07420001B2
Source datasetuspto-grants-2008_09
ORD IDord-f1f60dd0a03346a4a85b8cbab9c2dfd6
Source noteuspto-grants-2008_09