HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2221086Generated: October 29, 2026
Methanol → tert-Butyl 5-phenylpyridin-2-ylcarbamate
https://huagongshe.com/reaction/2221086
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Phenylboronic Acid | HCID 66827 | — |
| Reactant | 2-(Boc-amino)-5-bromopyridine | HCID 16217843 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | tert-Butyl 5-phenylpyridin-2-ylcarbamate | HCID 58671538 | 72% |
Reaction Steps
To a solution of 1B (7.65 g, 28 mmol) in THF (50 mL)-MeOH (50 mL) at RT was added phenylboronic acid (6.83 g, 56 mmol), PXPd (500 mg, 0.93 mmol), followed by K2CO3 (15.5 g, 112 mmol). The reaction mixture was stirred at 70° C. in a preheated oil bath for 1 h. After this time, the reaction mixture was cooled to RT. The reaction mixture was poured into water (100 mL), and the resultant mixture was extracted with EtOAc (3×100 mL). The combined organic layers were washed with saturated NaCl. The organic layer was dried (Na2SO4), filtered and concentrated. The resulting residue was purified by silica gel (120 g) column chromatography eluting with a gradient of EtOAc (0-60%) in hexane to give the title compound as an off-white solid (5.4 g, 72%). LC/MS (method A): retention time=3.07 min, (M+H)+=271.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07368458B2 |
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| Source dataset | uspto-grants-2008_05 |
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| ORD ID | ord-89b5d69a5aa34010b45e5ccad462765b |
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| Source note | uspto-grants-2008_05 |
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