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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 544930Generated: October 30, 2026

Hydrochloric Acid → HCID 24985577, compound

https://huagongshe.com/reaction/544930

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium CarbonateHCID 11430—
Reactant(R)-(-)-2,2-Dimethyl-1,3-dioxolan-4-ylmethyl p-ToluenesulfonateHCID 6993835—
ReactantHCID 59761472HCID 59761472—
SolventMethanolHCID 887—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 24985577HCID 2498557731.1%

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of N-(5-(cyclopropylcarbamoyl)-2-methylphenyl)-5-(3-hydroxyphenyl)thiophene-2-carboxamide (Example 144, 80 mg, 0.20 mmol), (R)-(−)-2,2-dimethyl-1,3-dioxolan-4-ylmethyl p-toluenesulfonate (70 mg, 0.24 mmol) and K2CO3 (84 mg, 0.61 mmol) in DMF (0.3 mL) was stirred and heated at 80° C. for 17 h. After cooling to rt, the mixture was diluted with water (˜5 mL) and extracted with EtOAc (3×10 mL) and the combined extracts were washed with brine, dried over anhyd. Na2SO4, filtered, and concentrated under vacuum to afford a brown oil. This material was purified by reverse-phase Prep HPLC to isolate the major product which was dissolved in MeOH (˜3 mL) and 2 N aq HCl (0.3 mL) was added. The solution was warmed to 65° C. for 45 min then cooled to rt and concentrated under vacuum to remove most of the MeOH. The resulting heterogeneous mixture was diluted with water (˜2-3 mL) and stirred for 1 h. The resulting solid was collected by vacuum filtration, rinsed with water (˜5 mL), and air dried in funnel then under vacuum to afford 29 mg (30%) of an off-white solid as the title compound (Example 193). HPLC Ret. Time=2.90 min, LCMS [M+H]+ 467.29.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07935696B2
Source datasetuspto-grants-2011_05
ORD IDord-7c465faaf92c4116917ae631694ea0c8
Source noteuspto-grants-2011_05