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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 81893Generated: October 30, 2026

4-Toluenesulfonyl chloride → HCID 69000171, compound

https://huagongshe.com/reaction/81893

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Toluenesulfonyl chlorideHCID 7397—
ReactantAmmonium HydroxideHCID 14923—
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantHCID 68997121HCID 68997121—
SolventDichloromethaneHCID 6344—
Solvent1,1-DichloroethaneHCID 6365—
SolventSodium chloride; waterHCID 57417360—
ProductHCID 69000171HCID 69000171—

Reaction Steps

3-Chloroperoxybenzoic acid (7.8 g of 77%) was added in a single portion to a solution of tert-butyl N-{4-[2-(2-methoxyethyl)-1H-imidazo[4,5-c][1,5]naphthyridin-1-yl]butyl}carbamate (7 g) in dichloroethane (100 mL). The reaction mixture was stirred at ambient temperature for 3 hours, Concentrated ammonium hydroxide (100 mL) was added and the reaction mixture was stirred until a suspension formed. Para-toluenesulfonyl chloride (3.6 g) was added in a single portion. The reaction mixture was stirred at ambient temperature for 2 hours and then diluted with dichloromethane and brine. The organic layer was separated, washed with brine (×2), dried over magnesium sulfate, filtered through a layer of CELITE filter aid, and then concentrated under reduced pressure to provide 8.83 g of crude tert-butyl N-{4-[4-amino-2-(2-methoxyethyl)-1H-imidazo[4,5-c][1,5]naphthyridin-1-yl]butyl}carbamate as a brown solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08846710B2
Source datasetuspto-grants-2014_09
ORD IDord-9ca1c1d8146446d5899c52c536e43a8c
Source noteuspto-grants-2014_09