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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1845963Generated: November 1, 2026

Triethylamine → HCID 66727301, compound

https://huagongshe.com/reaction/1845963

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantEthyl chloroformateHCID 10928—
ReactantN-(tert-butoxycarbonyl)-2-aminoethanethiolHCID 3017761—
ReactantHCID 66727336HCID 66727336—
SolventDichloromethaneHCID 6344—
ProductHCID 66727301HCID 66727301—

Reaction Steps

320 mg of (S)-6-(4-tert-butoxycarbonyl-2-methyl-1,4-diazepan-1-ylsulfonyl)isoquinoline 2-oxide was dissolved in dichloromethane, and 0.1 mL of ethyl chlorocarbonate, 0.42 mL of 2-(N-tert-butoxycarbonylamino)ethanethiol, and 0.21 mL of triethylamine were added at 0° C. The reaction solution was stirred at room temperature for 16 hours and then concentrated under reduced pressure, and the obtained crude product was purified by silica gel column chromatography (hexane:acetone=4:1) to obtain 223 mg of the compound of interest as a colorless oil (51%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08951997B2
Source datasetuspto-grants-2015_02
ORD IDord-6090e760212e40269a29ad6e686bfa9c
Source noteuspto-grants-2015_02