HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1431977Generated: November 3, 2026
3-Pyridinylboronic acid → HCID 68615877, compound
https://huagongshe.com/reaction/1431977
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-Pyridinylboronic acid | HCID 2734378 | — |
| Reactant | HCID 68615727 | HCID 68615727 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Product | HCID 68615877 | HCID 68615877 | 13.6% |
Reaction Steps
A mixture of 4-bromo-1-tert-butoxycarbonyl-2-(3,4,5-trimethoxyphenyl)-pyrrole (2.0 g, 5.0 mmol, Example 76b), Pd(PPh3)4 (290 mg, 0.25 mmol) and pyridine-3-boronic acid (614 mg, 5.0 mmol) are evacuated for 10 min and set under argon atmosphere, followed by addition of degassed dimethoxyethane (DME, 10 ml) and 2 M aqueous Na2CO3 solution (10 ml). The reaction mixture is heated for 20 h to 80° C., cooled to room temperature and diluted with water and ethyl acetate. The organic layer is dried (MgSO4), filtered and the solvents are evaporated. The residue is chromatographed with ethyl acetate/hexane (1:1) to yield first 1-tert-butoxycarbonyl-4-(3-pyridyl)-2-(3,4,5-trimethoxy-phenyl)-pyrrole (280 mg, 12%) as a yellowish amorphous solid and then the title compound (700 mg, 45%) as a yellowish solid, 1H-NMR (300 MHz, DMSO-d6): 11.52 (br.s, 1H); 7.88 (br. s, 1H); 8.33 (br.d; J=6.0, 1H); 8.0-7.95 (m, 1H); 7.48 (br.s, 1H); 7.35-7.3 (m, 1H); 7.07 (br.s, 1H); 7.02 (s, 2H); 3.85 (s, 2MeO); 3.67 (s, MeO).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07612064B2 |
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| Source dataset | uspto-grants-2009_11 |
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| ORD ID | ord-a672f3078bc14e7389037ae43f89c682 |
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| Source note | uspto-grants-2009_11 |
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