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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 337420Generated: October 30, 2026

Pyridine → HCID 23144205, compound

https://huagongshe.com/reaction/337420

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantThionyl ChlorideHCID 24386—
Reactant1-(dimethylcarbamoyl)piperidine-4-carboxylic acidHCID 5076474—
Reactant2-Amino-4-(2-furyl)-5-morpholinothiazoleHCID 23144158—
SolventDichloromethaneHCID 6344—
ProductHCID 23144205HCID 2314420581%

Reaction Steps

1-(N,N-dimethylcarbamoyl)piperidine-4-carboxylic acid (300 mg, 1.50 mmol) obtained in Step 2 was dissolved in dichloromethane (15 mL), and thionyl chloride (0.547 mL, 7.50 mmol) was added thereto, followed by stirring under heating and reflux for 1 hour. The reaction mixture was concentrated under reduced pressure, and the resulting residue was dissolved in chloroform (5 mL). The resulting solution was added to a pyridine (10 mL) solution of 2-amino-4-(2-furyl)-5-morpholinothiazole (126 mg, 0.50 mmol) obtained in Step 1 of Example 29, 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 (ethyl acetate:methanol=9:1) to afford the entitled Compound 55 (171 mg, 81%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08889718B2
Source datasetuspto-grants-2014_11
ORD IDord-0d329a6341c44218958e04b9a8dfb8e8
Source noteuspto-grants-2014_11