Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 227492Generated: November 1, 2026

Triethylamine → HCID 10453790, compound

https://huagongshe.com/reaction/227492

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantHCID 10314224HCID 10314224—
SolventAcetonitrile methylene chlorideHCID 21877088—
ProductHCID 10453790HCID 10453790—

Reaction Steps

To a solution of 5-hydroxy-3-(morpholin-4-ylsulfonyl)-1H-indole-2-carboxamide from Example 50 (37 mg, 0.12 mmol) in 3 mL of dichloromethane/acetonitrile (1:1) was added triethylamine (0.048 mL, 0.34 mmol) and methanesulfonyl chloride (0.0098 mL, 0.13 mmol). After one hour, another portion of methanesulfonyl chloride (0.005 mL) was added. After another 10 minutes, the mixture was partitioned between ethyl acetate and saturated NH4Cl solution, and the organic layer was washed with saturated NaHCO3 solution and brine, dried (Na2SO4), filtered, and concentrated in vacuo. The resulting solid was triturated with acetonitrile/methanol (1:1) to give the titled compound as a white solid. Proton NMR for the product was consistent with the titled compound. HRMS (ES) exact mass calculated for C14H18N3O7S2 (M+H+): 404.0581. Found 404.0620.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07560546B2
Source datasetuspto-grants-2009_07
ORD IDord-f109355d719549dd87f34506e4f69f4b
Source noteuspto-grants-2009_07