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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1599089Generated: November 3, 2026

Ammonium nitrate → 2-(3-Amino-2,4-dioxo-2,3,4,5-tetrahydro-benzo[b][1,4]diazepin-1-yl)-N-isopropyl-N-(4-methoxy-phenyl)-acetamide

https://huagongshe.com/reaction/1599089

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium nitrateHCID 22985—
Reactant2-[3-Amino-5-(4-methoxybenzyl)-2,4-dioxo-2,3,4,5-tetrahydro-benzo[b][1,4]diazepin-1-yl]-N-isopropyl-N-(4-methoxyphenyl)-acetamideHCID 18929590—
SolventAcetonitrile--water (1/1)HCID 18373917—
Product2-(3-Amino-2,4-dioxo-2,3,4,5-tetrahydro-benzo[b][1,4]diazepin-1-yl)-N-isopropyl-N-(4-methoxy-phenyl)-acetamideHCID 1892957397.6%

Reaction Steps

To a stirred solution of 2-[3-Amino-5-(4-methoxybenzyl)-2,4-dioxo-2,3,4,5-tetrahydro-benzo[b][1,4]diazepin-1-yl]-N-isopropyl-N-(4-methoxyphenyl)-acetamide (2.63 g, 5.09 mmol) in acetonitrile/H2O (9:1, 70 mL) at ambient temperature was added cerric ammonium nitrate (10.05 g, 18.3 mmol) portionwise over one hour. The solution was stirred overnight at room temperature. The solution was concentrated in vacuo, chased with toluene (2×50 mL) and the residue was extracted with CH2Cl2 (3×50 mL), filtered and concentated to an orange glass. The crude product was purified by flash chromatography on silica gel (100 g) eluting successively with CH2 Cl2 /CH3OH (15:1, 1.5 L) and CH2Cl2 /CH3OH (10:1, 1.3 L). Appropriate fractions were combined and concentrated under reduced pressure to give the title compound (1.97 g, 4.97 mmol) as a brown foam: 1H NMR (300 MHz, DMSO-d6): d 10.68 (br s, 1H), 7.39-6.98 (m, 8H), 5.75 (s, 1H), 4.76 (m, 1H), 4.16-3.92 (m, 4H), 3.7 (s, 3H), 3.15 (m, 2H), 0.97 (m, 6H); TLC (CH2Cl2 /CH3OH (13:1)): Rf =0.21.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05739129
Source datasetuspto-grants-1998_04
ORD IDord-d071d168adaf4af0b784dd036badba19
Source noteuspto-grants-1998_04