Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 931601Generated: October 30, 2026

4-Nitrobenzoyl isothiocyanate → N-((7-bromo-3-chloro-5-(2-hydroxyethyl)-5H-chromeno[2,3-c]pyridin-5-yl)carbamothioyl)-4-nitrobenzamide

https://huagongshe.com/reaction/931601

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Nitrobenzoyl isothiocyanateHCID 141398—
ReactantHCID 77230928HCID 77230928—
SolventTetrahydrofuranHCID 8028—
ProductN-((7-bromo-3-chloro-5-(2-hydroxyethyl)-5H-chromeno[2,3-c]pyridin-5-yl)carbamothioyl)-4-nitrobenzamideHCID 86658374112.7%

Reaction Steps

A reaction mixture of 2-(5-amino-7-bromo-3-chloro-5H-chromeno[2,3-c]pyridin-5-yl)ethanol (2.8 g, 7.87 mmol) and 4-nitrobenzoyl isothiocyanate (1.639 g, 7.87 mmol) in THF (100 mL) was stirred at RT for 1 hour. The reaction mixture was then concentrated under reduced pressure to afford N-(7-bromo-3-chloro-5-(2-hydroxyethyl)-5H-chromeno[2,3-c]pyridin-5-ylcarbamothioyl)-4-nitrobenzamide (5 g, 8.87 mmol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09296759B2
Source datasetuspto-grants-2016_03
ORD IDord-1e0662b7ce774e4a85493b0fe3ba85e0
Source noteuspto-grants-2016_03