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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 551107Generated: October 30, 2026

Sodium Bicarbonate → HCID 57663751, compound

https://huagongshe.com/reaction/551107

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 67172944HCID 67172944—
ReactantHCID 67173624HCID 67173624—
SolventEthanolHCID 702—
ProductHCID 57663751HCID 57663751—

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of 1-ethoxy-2-(6-methyl-2,5-dioxo-5,6-dihydro-4H-imidazo[1,5,4-de]quinoxalin-1(2H)-yl)ethaniminium chloride from Step B (72 mg, 0.22 mmol) and (2S)-5-(2-aminoethyl)-6-nitro-1,3-dihydrospiro[indene-2,3′-pyrrolo[2,3-b]pyridin]-2′(1′H)-one (73 mg, 0.25 mmol, described in Intermediate 15) in EtOH (7 mL) was heated to 100° C. for 5 min then allowed to cool. The reaction was poured into dilute aqueous NaHCO3 (50 mL) and the mixture was extracted with EtOAc (100 mL). The organic layer was washed with brine, dried over Na2SO4, filtered, and concentrated under reduced pressure. The crude product was purified by silica gel chromatography, eluting with a gradient of CH2Cl2:MeOH—100:0 to 80:20, to give the title compound. MS: 71/Z=520 (M+1) HRMS: m/z=520.2081; calculated m/z=520.2092 for C29H26N7O3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07947677B2
Source datasetuspto-grants-2011_05
ORD IDord-c1512c335f2e4aa3b9633b55d04a29c4
Source noteuspto-grants-2011_05