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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1916648Generated: November 2, 2026

Triethylamine → HCID 10048913, compound

https://huagongshe.com/reaction/1916648

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant4-MethylpiperidineHCID 69381—
ReactantHCID 67363469HCID 67363469—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 10048913HCID 10048913—

Reaction Steps

32 μL (0.40 mmol) methanesulphonic acid chloride are added to a solution of 100 mg (0.28 mmol) {5-[5-(4-chloro-phenyl)-pyridin-2-ylethynyl]-benzofuran-2-yl}-methanol and 69 μL (0.50 mmol) triethylamine in 5 mL DCM at 0° C. and the reaction is stirred for 1 h at this temperature. Another 70 μL (0.89 mmol) methanesulphonic acid chloride are added and the reaction is stirred overnight at RT. Then 0.24 ml (2.00 mmol) 4-methylpiperidine is added and the reaction is stirred for 2 hours at RT. The reaction solution is diluted with water and the aqueous phase extracted twice with DCM. The organic phase is dried over MgSO4 and the solvent is eliminated i.vac. The purification is carried out by column chromatography on silica gel (DCM/methanol 9:1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08618132B2
Source datasetuspto-grants-2013_12
ORD IDord-9b6e8c4d2a524524bbdfcb8491fc7c25
Source noteuspto-grants-2013_12