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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1647766Generated: October 31, 2026

Triethylamine → HCID 67808141, compound

https://huagongshe.com/reaction/1647766

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantEthanesulfonyl chlorideHCID 11667—
Reactant5-AminoindoleHCID 78867—
SolventDichloromethaneHCID 6344—
ProductHCID 67808141HCID 6780814199.1%

Reaction Conditions

Temperature23 °C

Reaction Steps

To a solution of 5-amino-1H-indole (10.0 g, 76 mmol) and triethylamine (15.8 mL, 114 mmol) in 100 mL CH2Cl2 at 0° C. was added dropwise a solution of ethanesulfonyl chloride (7.9 mL, 83 mmol) in 25 mL of CH2Cl2. The solution was allowed to slowly warm to 23° C. over 20 h. The reaction mixture was concentrated in vacuo and the residue dissolved in 400 mL of ethyl acetate. The organic layer was washed with 100 mL of water, 50 mL of 0.1 M HCl, 50 mL of saturated NaHCO3 solution, and 50 mL of saturated NaCl solution. The organic layer was dried over anhydrous K2CO3, filtered, and concentrated in vacuo to obtain 5-ethanesulfonyl-amino-1H-indole (16.9 g, >99%) which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05434154
Source datasetuspto-grants-1995_07
ORD IDord-6fd02c75e72c4ca6a518750a91b61ccb
Source noteuspto-grants-1995_07