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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 226923Generated: October 30, 2026

Sodium Hydroxide → HCID 178425691, compound

https://huagongshe.com/reaction/226923

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantHCID 57754544HCID 57754544—
ReactantAzidomethyl N-(1,1-dimethylethyl)carbamateHCID 57754756—
CatalystCopperHCID 23978—
CatalystCopper sulfate pentahydrateHCID 24463—
SolventWaterHCID 962—
Solventtert-ButanolHCID 6386—
ProductHCID 178425691HCID 17842569154.6%

Reaction Conditions

Temperature80 °C

Reaction Steps

29 mg (0.092 mmol) of 3-(3,4-dimethyl-benzoyl)-1-prop-2-ynyl-1H-quinolin-4-one 4c (prepared as described by Paine, J. B.; J. Het. Chem. 1987, 351), 19 mg (0.11 mmol) of tert-butyl-carbamic acid azidomethyl ester, 5.0 mg (0.078 mmol) of copper powder, and 2.0 mg (0.008 mmol) of copper(II) sulfate pentahydrate were combined in a mixture of 0.5 mL tert-butanol and 0.2 mL water and stirred at 80° C. for 4 h. Then 70 mg (1.75 mmol) of sodium hydroxide in 1 mL water was added to that mixture and the resultant mixture was stirred at 80° C. for another hour. The mixture was filtered and purified using reverse phase HPLC (mobile phase with a gradient 15-80% acetonitrile in 50 min). Lyophilization of the HPLC fractions containing purified 4d provided 18 mg of a pale yellow product as the trifluoroacetate salt: LC-MSD, m/z for C21H18N4O2, [M+H]+=359.5, HPLC retention time: 1.5 min; 1H NMR (400 MHz, CDCl3): δ 2.25 (s, 3H), 2.3 (s, 3H), 6.7 (s, 2H), 7.1-7.2 (m, 1H), 7.4-7.45 (m, 1H), 7.45-7.5 (m, 2H), 7.75-7.85 (m, 3H), 8.4-8.5 (m, 1H), 8.65 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07557213B2
Source datasetuspto-grants-2009_07
ORD IDord-3ddd6766cee245278f0e601b2226573b
Source noteuspto-grants-2009_07