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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2047243Generated: October 30, 2026

Thionyl Chloride → HCID 60142727, compound

https://huagongshe.com/reaction/2047243

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
ReactantSodium methanethiolateHCID 4378561—
ReactantHCID 68153033HCID 68153033—
SolventDichloromethaneHCID 6344—
ProductHCID 60142727HCID 601427279.4%

Reaction Steps

3-(2-chloro-6-fluorophenyl)-5-(1-(pyridin-3-yl)-5-(trifluoromethyl)-1H-pyrazol-4-yl)isoxazole-4-carboxylic acid (30 mg, 0.066 mmol) was treated with thionylchloride (1.5 mL) and stirred at reflux for 2 h. The mixture was concentrated under reduced pressure. The intermediate was treated with benzene (3×) and the benzene was evaporated to remove water. Then, the obtained mixture was dissolved in benzene (1.5 mL) and sodium methanethiolate (32.5 mg, 0.46 mmol) was added. The reaction mixture was stirred at reflux for 5 h. The mixture was diluted with dichloromethane and washed with water (3×), dried over sodium sulfate, filtered and concentrated under reduced pressure. The product (example B-68) was purified by pTLC (1:1 EE/PE) to give 3 mg of a white solid (yield 9%). Result of LC/MS MH+: 482.76; 1H NMR (CDCl3): 2.33 (t, 3H), 7.19 (t, 1H), 7.33-7.55 (m, 6H), 8.23 (s, 1H)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08592456B2
Source datasetuspto-grants-2013_11
ORD IDord-f6d8f0acf3c144faa22847ea868d6997
Source noteuspto-grants-2013_11