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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 716377Generated: October 25, 2026

Triphenyl phosphite → HCID 58324498, compound

https://huagongshe.com/reaction/716377

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenyl phosphiteHCID 7540—
Reactantmethyl 6-(2-(methoxycarbonyl)-1H-pyrrol-1-yl)-5-nitronicotinateHCID 58324515—
CatalystPlatinumHCID 23939—
CatalystAmmonium metavanadateHCID 516859—
SolventDichloromethaneHCID 6344—
ProductHCID 58324498HCID 5832449854%

Reaction Steps

Methyl 6-(2-(methoxycarbonyl)-1H-pyrrol-1-yl)-5-nitronicotinate (5.00 g, 16.38 mmol) was dissolved in dichloromethane (Volume: 82 ml) and to this solution was added triphenyl phosphite (0.051 g, 0.164 mmol), ammonium metavanadate (0.115 g, 0.983 mmol) and Pt/C (5% wt.) (0.639 g, 0.164 mmol). The reaction mixture was hydrogenated at 100 psi at 25° C. for 36 h. The reaction mixture was filtered through a short plug of celite and the plug and precipitate were washed well with methanol (100 mL) and then MeOH:DCM (100 mL, 1:1). The solids (celite and Pt/C) were continuously extracted with MeOH/DCM mixture (1:1) in a Soxlet extractor for 2 d. The extracts were combined with the earlier filtrates, concentrated in vacuo, crystallized with MeOH (100 mL) and the resulting solid was filtered off and suspended in ethyl ether (200 mL). The solid were filtered off and dried in vacuum to afford methyl 6-oxo-5,6-dihydropyrido[3,2-e]pyrrolo[1,2-a]pyrazine-3-carboxylate (2.15 g, 8.84 mmol, 54.0% yield) as a grey solid. 1H NMR (DMSO-d6) δ 11.49 (s, 1H), 8.69 (s, 1H), 8.15 (br. s., 1H), 8.11 (s, 1H), 7.16 (d, J=2.5 Hz, 1H), 6.78 (t, J=3.0 Hz, 1H), 3.91 (s, 3H). [M+H] calc'd for C12H9N3O3, 244. found, 244.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09187497B2
Source datasetuspto-grants-2015_11
ORD IDord-cb79a3d4939346499ae85c6d76b53849
Source noteuspto-grants-2015_11