HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-(Carboxymethyl)benzeneboronic acid → [2'-(1-tert-Butoxycarbonylamino-ethyl)-5'-(pyridin-4-ylcarbamoyl)-biphenyl-3-yl]-acetic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-(Carboxymethyl)benzeneboronic acid | HCID 22480132 | — |
| Reactant | {1-[2-Bromo-4-(pyridine-4-ylcarbamoyl)-phenyl]-ethyl}-carbamic acid tert-butyl ester | HCID 67408319 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Dimethoxyethane ethanol | HCID 20074477 | — |
| Product | [2'-(1-tert-Butoxycarbonylamino-ethyl)-5'-(pyridin-4-ylcarbamoyl)-biphenyl-3-yl]-acetic acid | HCID 68245521 | — |
Reaction Conditions
| Temperature | 160 °C |
|---|
Reaction Steps
To a solution of {1-[2-bromo-4-(pyridine-4-ylcarbamoyl)-phenyl]ethyl}-carbamic acid tert-butyl ester (1951 μmol) in a mixture of DME/EtOH/2N Na2CO3: 1/1/1 (10 ml) were added 3-carboxymethylphenylboronic acid (1.5 eq) and Pd tetrakis (0.05 eq). The reaction mixture was heated in the microwave at 160° C. for 15 minutes. The reaction mixture was cooled to RT, filtered over celite and washed with EtOAc and MeOH. The solvents were removed under reduced pressure. The compound was purified by column chromatography (silicagel, DCM/MeOH gradient).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08912209B2 |
| Source dataset | uspto-grants-2014_12 |
| ORD ID | ord-7ff7fb8da371437fbade0991adf50876 |
| Source note | uspto-grants-2014_12 |