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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1776921Generated: October 29, 2026

Triethylamine → HCID 86728297, compound

https://huagongshe.com/reaction/1776921

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant3-Chloropropanesulphonyl chlorideHCID 15410—
ReactantHCID 86728298HCID 86728298—
SolventDichloromethaneHCID 6344—
ProductHCID 86728297HCID 86728297104.4%

Reaction Conditions

Temperature12 °C

Reaction Steps

To a solution of 6-amino-5-(11-fluoro-6H-pyrido[2′,3′:5,6][1,3]oxazino[3,4-a]indol-2-yl)-2-(4-fluorophenyl)-N-methylbenzofuran-3-carboxamide (70 mg, 0.13 mmol) and Et3N (0.1 mL) in CH2Cl2 (2 mL) was added 3-chloropropane-1-sulfonyl chloride (140 mg, 0.92 mmol) dropwise at 0° C. The reaction mixture was stirred at 12° C. for 16 hours. The reaction mixture was concentrated to provide 6-(3-chloropropylsulfonamido)-5-(11-fluoro-6H-pyrido[2′,3′:5,6][1,3]oxazino[3,4-a]indol-2-yl)-2-(4-fluorophenyl)-N-methylbenzofuran-3-carboxamide (90 mg, yield: 100%), which was used directly in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09265773B2
Source datasetuspto-grants-2016_02
ORD IDord-27ab14fd7a154a32aaf792a8b6969982
Source noteuspto-grants-2016_02