HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 337410Generated: October 26, 2026
Thionyl Chloride → 2-Chloro-N-[4-(2-furyl)-5-morpholinothiazol-2-yl]pyridine-4-carboxamide
https://huagongshe.com/reaction/337410
Participants
| Role | Name | HCID | Charge |
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| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 2-Chloroisonicotinic acid | HCID 236985 | — |
| Reactant | 2-Amino-4-(2-furyl)-5-morpholinothiazole | HCID 23144158 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | 2-Chloro-N-[4-(2-furyl)-5-morpholinothiazol-2-yl]pyridine-4-carboxamide | HCID 23144123 | 66% |
Reaction Steps
2-Chloroisonicotinic acid (5.00 g, 31.7 mmol) was added to thionyl chloride (40 mL), followed by stirring under heating and reflux for 2 hours. The reaction mixture was concentrated under reduced pressure, and the resulting residue was dissolved in dichloromethane (1 mL). The resulting solution was added to a pyridine (16 mL) solution of 2-amino-4-(2-furyl)-5-morpholinothiazole (880 mg, 5.00 mmol) obtained in Step 1 of Example 29, and then N,N-dimethylaminopyridine (48.8 mmol, 0.400 mmol) was added thereto, followed by stirring at room temperature for 1 hour. The reaction mixture was concentrated under reduced pressure, and the resulting residue was purified through silica gel column chromatography (hexane:ethyl acetate=1:3 to ethyl acetate) to afford the entitled Compound 39 (1.05 g, 66%)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08889718B2 |
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| Source dataset | uspto-grants-2014_11 |
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| ORD ID | ord-158185b6cf154fba846b68b5752c0c0c |
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| Source note | uspto-grants-2014_11 |
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