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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 60217Generated: October 30, 2026

Phosphorus pentachloride → 9-Benzenesulfonyl-3-bromo-5-chloro-9H-diprido[2,3-b;4',3'-d]pyrrole-6-carbonitrile

https://huagongshe.com/reaction/60217

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphorus pentachlorideHCID 24819—
Reactant8-(Benzenesulfonyl)-12-bromo-3-hydroxy-5,8,10-triazatricyclo[7.4.0.02,7]trideca-1(9),2,4,6,10,12-hexaene-4-carbonitrileHCID 58266472—
SolventDichloromethaneHCID 6344—
SolventChlorobenzeneHCID 7964—
Product9-Benzenesulfonyl-3-bromo-5-chloro-9H-diprido[2,3-b;4',3'-d]pyrrole-6-carbonitrileHCID 5836512853%

Reaction Steps

A solution of 9-benzenesulfonyl-3-bromo-5-hydroxy-9H-dipyrido[2,3-b;4′,3′-d]pyrrole-6-carbonitrile (2.0 g, 4.66 mmol) and phosphorus pentachloride (2.9 g, 14.0 mmol) in chlorobenzene (6 mL) was heated at 105° C. for 1 hour. The reaction mixture was cooled to ambient temperature and the solvent removed in vacuo to afford a residue. The resultant residue was dissolved in dichloromethane (300 mL) and the solution was treated with ice/water (300 mL). The layers were separated and the aqueous layer further extracted with dichloromethane (300 mL). The combined organic layer was washed with brine, dried (Na2SO4), filtered and evaporated. The resultant residue was triturated with methanol and dried to afford the title compound as a tan solid (1.1 g, 53%). 1H NMR (300 MHz, DMSO-d6): 9.70 (s, 1H), 9.06 (d, J=2.2 Hz, 1H), 8.98 (d, J=2.2 Hz, 1H), 8.27-8.22 (m, 2H), 7.77-7.76 (m, 1H), 7.67-7.60 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09440976B2
Source datasetuspto-grants-2016_09
ORD IDord-41a5125f489f4b08bc538b7c3814b433
Source noteuspto-grants-2016_09