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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1969964Generated: October 30, 2026

Benzenesulfonyl chloride → HCID 86627488, compound

https://huagongshe.com/reaction/1969964

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzenesulfonyl chlorideHCID 7369—
ReactantTriethylamineHCID 8471—
ReactantHCID 86627489HCID 86627489—
SolventDimethylformamideHCID 6228—
ProductHCID 86627488HCID 8662748857%

Reaction Conditions

Temperature40 °C

Reaction Steps

62 μL (0.44 mmol) of triethylamine and then 31 μL (0.24 mmol) of benzenesulfonyl chloride are added to 60 mg (0.22 mmol) of 8-amino-4-oxo-4,5-dihydro-3H-pyrrolo[2,3-c]quinoline-1-ethyl carboxylate (synthesis 64) suspended in anhydrous dimethylformamide (1 mL). The solution is stirred for 1 h at 40° C. The solvent is evaporated and the raw product obtained is purified by recrystallization from methanol to give 51 mg (57%) of 8-benzenesulfonylamino-4-oxo-4,5-dihydro-3H-pyrrolo[2,3-c]quinoline-1-ethyl carboxylate in the form of a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08426437B2
Source datasetuspto-grants-2013_04
ORD IDord-b6d05c2f40e045a4a84ee4ae73b74247
Source noteuspto-grants-2013_04