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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1253011Generated: October 25, 2026

Water → 9-Chloro-7-[2-(2,4-di-t-amylphenoxy)butanoylamino]-6-hydroxy-1,5-benzodiazepin-2,4-dione

https://huagongshe.com/reaction/1253011

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantAmmonium ChlorideHCID 25517—
Reactant2-(2,4-Bis(1,1-dimethylpropyl)phenoxy)butyryl chlorideHCID 170393—
Reactant2-Amino-4-chloro-5-nitrophenolHCID 3894848—
SolventIsopropanolHCID 3776—
SolventAcetonitrileHCID 6342—
Product9-Chloro-7-[2-(2,4-di-t-amylphenoxy)butanoylamino]-6-hydroxy-1,5-benzodiazepin-2,4-dioneHCID 135583124—

Reaction Steps

20 g of 2-amino-4-chloro-5-nitrophenol was dispersed in 150 ml of acetonitrile, and 37.7 g of 2-(2,4-di-t-amylphenoxy)butanoyl chloride was added thereto dropwise under refluxing. After stirring while refluxing for 1 hour, the reaction mixture was cooled to room temperature, and the crystals thus formed were collected by filtration, washed with acetonitrile, and dried to obtain crystals weighing 49.5 g. A mixture of 49 g of the resulting crystals, 28 g of reduced iron, 2.7 g of ammonium chloride, 50 ml of water, and 500 ml of isopropanol was stirred while refluxing for 1 hour. The iron powder was removed by filtration, and the filtrate was cooled to precipitate crystals, which were then collected by filtration and dried to provide 42.4 g of the desired compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04746602
Source datasetuspto-grants-1988_05
ORD IDord-1cba715718e34875ad2b96e5a10929bb
Source noteuspto-grants-1988_05