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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1969976Generated: October 30, 2026

N-Acetylsulfanilyl chloride → HCID 86627501, compound

https://huagongshe.com/reaction/1969976

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-Acetylsulfanilyl chlorideHCID 8481—
ReactantHCID 68937404HCID 68937404—
SolventMethanolHCID 887—
ProductHCID 86627501HCID 8662750138%

Reaction Steps

This compound is prepared according to synthesis 43, from 60 mg (0.20 mmol) of 8-amino-4-oxo-4,5-dihydro-3H-pyrrolo[2,3-c]quinoline-1-ethyl carboxylate hydrochloride (synthesis 64) and 50 mg (0.21 mmol) of 4-acetylamino-benzenesulfonyl chloride. After trituration in hot methanol, 35 mg (38%) of 8-(4-acetylamino-benzenesulfonylamino)-4-oxo-4,5-dihydro-3H-pyrrolo[2,3-c]quinoline-1-ethyl carboxylate is obtained in the form of an orange-brown solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08426437B2
Source datasetuspto-grants-2013_04
ORD IDord-1ced3f229d4f44849f6950ea485e1133
Source noteuspto-grants-2013_04