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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 9387Generated: October 25, 2026

Potassium Carbonate → Tert-butyl [4-(3-amino-7-bromoquinolin-4-ylamino)butyl]carbamate

https://huagongshe.com/reaction/9387

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantSodium DithioniteHCID 24489—
ReactantTert-butyl [4-(7-bromo-3-nitroquinolin-4-ylamino)butyl]carbamateHCID 21984414—
Catalyst1,1'-Diethyl-4,4'-bipyridinium dibromideHCID 11474262—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductTert-butyl [4-(3-amino-7-bromoquinolin-4-ylamino)butyl]carbamateHCID 2198417499%

Reaction Steps

A solution of sodium hydrosulfite (43.35 g, 249 mmol) and potassium carbonate (38.28 g, 277 mmol) in water (300 mL) was added to a mixture of tert-butyl[4-(7-bromo-3-nitroquinolin-4-ylamino)butyl]carbamate (24.3 g, 55.3 mmol) and 1,1′-diethyl-4,4′-bipyridinium dibromide (1.03 g, 2.76 mmol) in dichloromethane (368 mL) and water (40 mL), and the reaction was stirred overnight at ambient temperature. The reaction mixture was filtered through a layer of CELITE filter aid. The aqueous filtrate was extracted with dichloromethane, and the combined organic fractions were dried over magnesium sulfate, filtered, and concentrated under reduced pressure to provide 22.4 g of tert-butyl[4-(3-amino-7-bromoquinolin-4-ylamino)butyl]carbamate as a brown powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07091214B2
Source datasetuspto-grants-2006_08
ORD IDord-ab593658aea3483d87d1ad57cc97e475
Source noteuspto-grants-2006_08