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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2423344Generated: October 31, 2026

Tetrahydrofuran → HCID 67244353, compound

https://huagongshe.com/reaction/2423344

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
Reactant4-(4,6-Dimethoxy-1,3,5-triazin-2-yl)-4-methylmorpholinium chlorideHCID 2734059—
ReactantN-[4-(aminomethyl)-2-fluorophenyl]methanesulfonamide hydrochlorideHCID 21097525—
ReactantHCID 67244312HCID 67244312—
SolventTriethylamineHCID 8471—
ProductHCID 67244353HCID 6724435318%

Reaction Steps

To the 50 ml of round bottom flask were put N-(4-aminomethyl-2-fluoro-phenyl)-methanesulfonamide hydrochloride (0.14 g, 0.55 mmol), 3-(4-t-butylphenyl)-but-2-enoic acid (1.0 eq, 0.12 g) and DMTMM (1.2 eq, 0.183 g). To this mixture was poured 25 ml tetrahydrofuran, added triethylamine (excess, 0.5 ml) and stirred 12 hours at room temperature. After confirming the completion of the reaction with TLC, the reaction mixture was extracted with ethylacetate, washed 1N HCl solution. The combined organic layer was dried over MgSO4, filtered and concentrated under reduced pressure. The obtained liquid was purified with column chromatography (n-hexane/ethyl acetate=1/1) to yield the title compound (41.5 mg)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07960584B2
Source datasetuspto-grants-2011_06
ORD IDord-f5528a5cb6a64b61b0a6aac44182f247
Source noteuspto-grants-2011_06