HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 59607539, compound → (R)-ethyl 4-(3'-aminobiphenyl-4-yl)-3-(4-methoxy-4-oxobutanamido)butanoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 59607539 | HCID 59607539 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | (R)-ethyl 4-(3'-aminobiphenyl-4-yl)-3-(4-methoxy-4-oxobutanamido)butanoate | HCID 59607780 | 91.6% |
Reaction Steps
A suspension of (R)-ethyl 3-(4-methoxy-4-oxobutanamido)-4-(3′-nitrobiphenyl-4-yl)butanoate (123 mg, 0.278 mmol) and Pd/C (59.2 mg, 0.028 mmol) in EtOH (2 ml) is allowed to stir under hydrogen at room temperature for 5.5 hours. The reaction mixture is filtered, and the solution is concentrated to give (R)-ethyl 4-(3′-aminobiphenyl-4-yl)-3-(4-methoxy-4-oxobutanamido)butanoate (105 mg); HPLC retention time=0.84 minutes (condition B); MS (m+1)=413.1; 1H NMR (400 MHz, CHLOROFORM-d) δ ppm 1.28 (t, J=7.2 Hz, 3 H) 2.41-2.65 (m, 6 H) 2.85-3.00 (m, 2 H) 3.67 (s, 3 H) 4.11-4.22 (m, 2 H) 4.46-4.54 (m, 1 H) 6.31 (br d, J=8.8 Hz, 1 H) 6.71-6.74 (m, 1 H) 6.95-7.02 (m, 2 H) 7.21-7.25 (m, 3 H) 7.48-7.50 (m, 2 H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08822534B2 |
| Source dataset | uspto-grants-2014_09 |
| ORD ID | ord-0d45e7304a924b5883edd1bb2cfd7e42 |
| Source note | uspto-grants-2014_09 |