HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1848335Generated: October 31, 2026
Potassium Carbonate → 2-(2-Cyclopropyl-8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-5-yl)-isonicotinonitrile
https://huagongshe.com/reaction/1848335
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Bromo-4-cyanopyridine | HCID 11735544 | — |
| Reactant | (2-Cyclopropyl-8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-5-yl)boronic acid | HCID 58074662 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Solvent | Sodium chloride; water | HCID 57417360 | — |
| Product | 2-(2-Cyclopropyl-8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-5-yl)-isonicotinonitrile | HCID 46830632 | — |
Reaction Steps
In a screw cap vial (2-cyclopropyl-8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-5-yl)boronic acid, compound 303, (26 mg, 0.1 mmol) was dissolved in DME (0.6 mL) and 1 M K2CO3 (0.2 mL) under argon. 2-Bromo-isonicotinonitrile (18 mg, 0.1 mmol) and Pd(PPh3)4 (6 mg, 0.005 mmol) were added. The suspension was shaken at 80° C. for 17 h after which brine was added, and the aqueous phase was extracted with DCM (×3). The combined organic phases were dried, filtered and concentrated. The crude product was purified by flash chromatography, eluent TBME:heptane 4:1->9:1. This afforded the title compound as a solid 1H NMR (300 MHz, DMSO) δ 9.23-9.09 (m, 1H), 9.00 (dd, J=4.9, 0.8 Hz, 1H), 7.95 (dd, J=4.9, 1.5 Hz, 1H), 7.90 (d, J=8.3 Hz, 1H), 7.24 (d, J=8.4 Hz, 1H), 4.03 (s, 3H), 2.29 (tt, J=8.1, 5.0 Hz, 1H), 1.18-0.87 (m, 4H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08952162B2 |
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| Source dataset | uspto-grants-2015_02 |
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| ORD ID | ord-1311d054ce174ccfbe05bfeefb60295b |
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| Source note | uspto-grants-2015_02 |
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