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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 23406Generated: October 29, 2026

Sodium Sulfate → 1-carbamoylmethyl-5-nitro-1H-indole-3-sulfonyl chloride

https://huagongshe.com/reaction/23406

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium SulfateHCID 24436—
ReactantChlorosulfonic acidHCID 24638—
Reactant(5-Nitro-indol-1-yl)-acetonitrileHCID 22574036—
SolventDichloromethaneHCID 6344—
Product1-carbamoylmethyl-5-nitro-1H-indole-3-sulfonyl chlorideHCID 2257398951%

Reaction Steps

Chlorosulfonic acid (3.05 ml, 45.9 mmole) from the above Step was added to a suspension of anhydrous sodium sulfate (0.71 g) in methylene chloride (30 ml). After stirring for 25 minutes at room temperature, (5-nitro-indol-1-yl)-acetonitrile (1.00 g) dissolved in methylene chloride was added via syringe. After stirring for 2 h, the reaction mixture was worked up by the cautious addition of ice. When the ice had melted, the mixture was filtered to afford an off-white powder which was washed well with water to afford 0.806 g of 1-carbamoylmethyl-5-nitro-1H-indole-3-sulfonyl chloride (51% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06852726B2
Source datasetuspto-grants-2005_02
ORD IDord-1c98694ec1084081892f94b60d78dd43
Source noteuspto-grants-2005_02