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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2234005Generated: October 29, 2026

Hydrochloric Acid → HCID 68581169, compound

https://huagongshe.com/reaction/2234005

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantThionyl ChlorideHCID 24386—
ReactantMethanesulfonamideHCID 72879—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
ReactantHCID 11463807HCID 11463807—
SolventTolueneHCID 1140—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 68581169HCID 68581169—

Reaction Steps

2-(4-{[(3,4-Dichloro-5-methyl-1H-pyrrol-2-yl)carbonyl]amino}piperidin-1-yl)-1,3-thiazole-5-carboxylic acid (Example 227; 0.160 g, 0.397 mmol) was suspended in toluene (3 ml) and thionyl chloride (0.288 ml, 3.97 mmol) was added dropwise at room temperature. The solution was refluxed for 1 h. Excess thionyl chloride and toluene were removed in vacuo. The precipitate formed was dissolved in dioxane and methane sulfonamide (0.075 g, 0.794 mmol) was added. The mixture was stirred at 100° C. for 0.5 h after which DBU (0.119 ml, 0.794 mmol) was added. The mixture was stirred for a further 1 h at room temperature was acidified with 10% HCl solution. The mixture was extracted with EtOAc and washed with water. The organic layer was dried over sodium sulfate and conc in vacuo. The crude mixture dissolved in DMSO, and was purified by reverse phase HPLC eluting with acetonitrile/water (0.1% TFA) to afford the desired product. (15 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07709503B2
Source datasetuspto-grants-2010_05
ORD IDord-18ef67326a644ab9b5aeb20f6da261b6
Source noteuspto-grants-2010_05