HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1443083Generated: October 31, 2026
Ethanol → 4-Chloro-2-methyl-7-pyridin-3-yl-thiazolo[4,5-c]pyridine
https://huagongshe.com/reaction/1443083
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethanol | HCID 702 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 3-Pyridinylboronic acid | HCID 2734378 | — |
| Reactant | 4-Chloro-7-iodo-2-methylthiazolo[4,5-c]pyridine | HCID 76850478 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 4-Chloro-2-methyl-7-pyridin-3-yl-thiazolo[4,5-c]pyridine | HCID 86612415 | — |
Reaction Steps
Tetrakis(triphenylphosphine)palladium(0) (52 mg, 0.05 mmol) was dissolved in 8 ml toluene. 4-Chloro-7-iodo-2-methyl-thiazolo[4,5-c]pyridine (280 mg, 0.90 mmol) (Example B), 3-pyridineboronic acid (133 mg, 1.08 mmol), 2M sodium carbonate (2.70 ml, 5.4 mmol) and 2 ml ethanol were added and the mixture stirred at 80° C. for 6 hrs. The reaction mixture was extracted with water and two times ethyl acetate. The organic extracts were washed with water and brine, dried with sodium sulfate, filtered and evaporated. The crude product was purified by flash chromatography on silica gel (heptane/ethyl acetate 9:1->0:100 gradient). The desired compound was obtained as a light yellow solid (100 mg, 42%), MS: m/e=263.1 (M+H+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07659401B2 |
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| Source dataset | uspto-grants-2010_02 |
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| ORD ID | ord-0bc404bf89b5471684ed443d92501cf1 |
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| Source note | uspto-grants-2010_02 |
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