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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1890412Generated: November 1, 2026

Ammonium Chloride → (+/-)-5-Amino-6-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-2,3,6,7-tetrahydro-[1,4]diazepine-1-carboxylic acid ethyl ester hydrochloride

https://huagongshe.com/reaction/1890412

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
Reactant(+/-)-6-(1,3-Dioxo-1,3-dihydro-isoindol-2-yl)-5-methoxy-2,3,6,7-tetrahydro-[1,4]diazepine-1-carboxylic acid ethyl esterHCID 68736156—
SolventMethanolHCID 887—
Product(+/-)-5-Amino-6-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-2,3,6,7-tetrahydro-[1,4]diazepine-1-carboxylic acid ethyl ester hydrochlorideHCID 6873523880%

Reaction Steps

To a solution of 39.00 g (112.93 mmol) of (+/−)-6-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-5-methoxy-2,3,6,7-tetrahydro-[1,4]diazepine-1-carboxylic acid ethyl ester dissolved in 350 mL of methanol was added 6.34 g (118.57 mmol) of ammonium chloride at room temperature. The resulting mixture was stirred under reflux for 12 h. The cooled solution was evaporated to remove solvent. The residue was triturated with diethyl ether and filtered to afford 33.00 g (80%) of (+/−)-5-Amino-6-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-2,3,6,7-tetrahydro-[1,4]diazepine-1-carboxylic acid ethyl ester hydrochloride (1:1) as a white powder. The compound was used as such in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08507476B2
Source datasetuspto-grants-2013_08
ORD IDord-6e2605d0e0124df390bc66462a30956d
Source noteuspto-grants-2013_08