HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 68711861, compound → HCID 11419551, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 68711861 | HCID 68711861 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Trifluoroacetic acid | HCID 6422 | — |
| Product | HCID 11419551 | HCID 11419551 | 84% |
Reaction Steps
N-({4′-[(1-benzofuran-2-ylcarbonyl)amino]-1,1′-biphenyl-4-yl}sulfonyl)glycine t-butyl ester (75 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 56 mg of N-({4′-[(1-benzofuran-2-ylcarbonyl)amino]-1,1′-biphenyl-4-yl}sulfonyl)glycine. LCMS MH+ (m/z) 451. 1H NMR (300 MHz, DMSO-d6): δ 10.54 ppm (s, 1H), 7.95-7.54 ppm (m, 11H), 7.34 ppm (dd, 1H, J1=7.5 Hz, J2=7.5 Hz), 7.20 ppm (dd, 1H, J1=7.5 Hz, J2=7.5 Hz), 3.42 ppm (d, 2H J=6.3 Hz).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07420001B2 |
| Source dataset | uspto-grants-2008_09 |
| ORD ID | ord-5ae43a7b3700478184b23106b1b94ce2 |
| Source note | uspto-grants-2008_09 |