Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1481813Generated: October 28, 2026

Ammonium nitrate → HCID 68357009, compound

https://huagongshe.com/reaction/1481813

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium nitrateHCID 22985—
ReactantHCID 86707877HCID 86707877—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
ProductHCID 68357009HCID 68357009—

Reaction Steps

To a solution of methyl 1′-(4-methoxybenzyl)-3′-methyl-2′,5′-dioxo-5,7-dihydrospiro[cyclopenta[b]pyridine-6,4′-imidazolidine]-3-carboxylate (100 mg, 0.25 mmol) in acetonitrile (8.4 mL) at ambient temperature was added eerie ammonium nitrate (4.1 g, 7.6 mmol) as a solution in H2O (5 mL). After 20 min, the reaction mixture was partitioned between H2O (50 mL) and 9:1—CH2Cl2:i-PrOH (50 mL). The aqueous was extracted further with 9:1—CH2Cl2:i-PrOH (5×50 mL) and the combined organic extracts were dried over sodium sulfate, filtered, and concentrated in vacuo. The crude solid was washed with MTBE (3×10 mL) then partitioned between saturated aqueous sodium bicarbonate (5 mL) and EtOAc (10 mL). The aqueous layer was extracted further with EtOAc (10 mL) and the combined organic extracts were dried over sodium sulfate, filtered, and concentrated in vacuo to provide the title compound in sufficient purity for use in the next step. MS: m/z 276.1 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09409916B2
Source datasetuspto-grants-2016_08
ORD IDord-0118e5e26f454a04b59b7c4af2604efd
Source noteuspto-grants-2016_08