HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1403671Generated: October 29, 2026
3-Aminophenylboronic acid → {1-[3'-Amino-5-(3-fluoro-pyridin-4-ylcarbamoyl)-biphenyl-2-yl]-ethyl}-carbamic acid tert-butyl ester
https://huagongshe.com/reaction/1403671
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3-Aminophenylboronic acid | HCID 92269 | — |
| Reactant | {1-[2-Bromo-4-(3-fluoro-pyridin-4-ylcarbamoyl)-phenyl]-ethyl}-carbamic acid tert-butyl ester | HCID 67407943 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Citric Acid | HCID 311 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethoxyethane ethanol | HCID 20074477 | — |
| Product | {1-[3'-Amino-5-(3-fluoro-pyridin-4-ylcarbamoyl)-biphenyl-2-yl]-ethyl}-carbamic acid tert-butyl ester | HCID 67422654 | — |
Reaction Steps
To a solution of {1-[2-bromo-4-(3-fluoro-pyridine-4-ylcarbamoyl)-phenyl]-ethyl}-carbamic acid tert-butyl ester (1094 μmol) and 3-aminophenylboronic acid (2 eq) in a mixture of DME/ethanol/1N Na2CO3: 1/1/1 (10 ml) was added Pd tetrakis (0.05 eq). The reaction mixture was heated in the microwave at 130° C. for 1.5 hours. The reaction mixture was cooled to RT and diluted with water and citric acid and extracted with EtOAc. The combined organic layers were washed with water and brine. The organic layer was dried over MgSO4 and the solvent was removed under reduced pressure. The compound was purified by column chromatography (silicagel, DCM/MeOH gradient).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08912209B2 |
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| Source dataset | uspto-grants-2014_12 |
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| ORD ID | ord-3a40cbd91e8641e2ac9b571f4eeeb15b |
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| Source note | uspto-grants-2014_12 |
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