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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1080215Generated: November 4, 2026

A-816719.1 → HCID 479584, compound

https://huagongshe.com/reaction/1080215

Reaction equation

Participants

RoleNameHCIDCharge
ReactantA-816719.1HCID 178073—
ReactantSodium AcetateHCID 517045—
ReactantdimethoxytetrahydrofuraneHCID 11788317—
SolventEthyl AcetateHCID 8857—
ProductHCID 479584HCID 479584—

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of 25 mg 8-(3(S)-aminopyrrolidinyl)-1-cyclopropyl-7-fluoro-9-methyl-4-oxo-4H-quinolizine-3-carboxylic acid hydrochloride (from Example 257) and 40 mg of sodium acetate in 0.7 mL of ethyl acetate was heated to 100° C. To this solution was added 0.009 mL of dimethoxytetrahydrofuran dropwise, and the reaction was stirred at 110° C. for 5 min, then quenched by addition of water. The mixture was extracted twice with methylene chloride, and the extract was washed with water, dried over MgSO4 and concentrated. The residue was purified by preparative TLC, eluting with 100:10 chloroform:methanol, to give 13.6 mg of the title product as a yellow solid after removal of the solvent. MS 395 (M-Cl)+. 1H NMR (CDCl3) δ: 0.67 (m, 2H), 1.00 (m, 2H), 2.20 (m, 1H), 2.46 (m, 1H), 2.56 (m, 1H), 2.66 (s, 3H), 3.89 (m, 1H), 3.99 (m, 2H0, 4.15 (m, 1H), 4.86 (m, 1H), 6.23 (t, 2H, J=2 Hz), 6.79 (t, 2H, J=2 hz), 8.32 (s, 1H), 9.15 (d, 1H, J=10 Hz), 13.83 (br, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05580872
Source datasetuspto-grants-1996_12
ORD IDord-3b78738826ca494097a79810660cfe08
Source noteuspto-grants-1996_12