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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 31090Generated: October 25, 2026

Potassium Sodium Tartrate → 4-Amino-8-bromo-N-ethyl-cinnoline-3-carboxamide

https://huagongshe.com/reaction/31090

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium Sodium TartrateHCID 9357—
ReactantAluminum(III) ChlorideHCID 6451240—
Reactant2-[(2-bromophenyl)-hydrazono]-N-ethyl-2-cyanoacetamideHCID 86613096—
SolventTolueneHCID 1140—
SolventEthyl AcetateHCID 8857—
Product4-Amino-8-bromo-N-ethyl-cinnoline-3-carboxamideHCID 6722867169.3%

Reaction Conditions

Temperature90 °C

Reaction Steps

To a stirred solution of 2-[(2-bromophenyl)-hydrazono]-N-ethyl-2-cyanoacetamide (260 mg, 0.88 mmol) in anhydrous toluene (10 mL) was added aluminum chloride (370 mg, 2.78 mmol). The reaction was heated with vigorous stirring at 90° C. for 1.5 hours, cooled, diluted with ethyl acetate (40 mL), and treated with Rochelle's salt (saturated aqueous solution). After stirring for 30 minutes, the organic layer was decanted into a separator funnel. (The white precipitate was rinsed with ethyl acetate three times.) The organic layer was washed with 1:1 brine:Rochelle's salt solution, dried over sodium sulfate, and concentrated to a light brown solid. The solid was slurred in ether and filtered to afford the title compound as a brown solid (180 mg, 69%). 1H NMR (300.132 MHz, CDCl3) δ 8.52 (s, 1H), 8.13 (dd, J=7.4, 1.1 Hz, 1H), 7.82 (dd, J=8.4, 1.1 Hz, 1H), 7.51 (dd, J=8.4, 7.5 Hz, 1H), 3.56 (dq, J=5.8, 7.3 Hz, 2H), 1.31 (t, J=7.3 Hz, 3H). MS APCI, m/z=395/397 (M+H). HPLC 1.90 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07425556B2
Source datasetuspto-grants-2008_09
ORD IDord-007e2dcc42ed49c4ba2ee43329806979
Source noteuspto-grants-2008_09