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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 748521Generated: October 28, 2026

Sodium hydride → HCID 136342113, compound

https://huagongshe.com/reaction/748521

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant5-Nitro-2-oxindoleHCID 230366—
ReactantEthyl 6-chloronicotinateHCID 2799611—
SolventWaterHCID 962—
SolventAmmonium ChlorideHCID 25517—
SolventDimethylazanideHCID 182180—
ProductHCID 136342113HCID 13634211347%

Reaction Conditions

Temperature135 °C

Reaction Steps

To a cooled solution of 5-nitrooxindol (5.27 g, 29.6 mmol) in N,N-dimethylamide (50 mL) was added sodium hydride (1.4 g, 35 mmol) during 5 min at 0° C. After 10 min at 0° C., 6-chloronicotinic acid ethyl ester (5.0 g, 26.9 mmol) was added dropwise and the reaction was heated to 135° C. for 45 min. The mixture was diluted with water (200 mL) and saturated NH4Cl(aq) (100 mL). The formed precipitate was filtrated and washed with water, methanol, ethyl acetate and diethyl ether. The residual green yellow solid was dried to give 4.1 g (47% yield) of the title compound: 1H NMR (DMSO-d6, 300 MHz) δ 14.57 (s, 1 H), 11.24 (s, 1 H), 8.73 (s, 1 H), 8.26 (s, 1 H), 8.10 (d, J=9 Hz, 1 H), 7.92 (d, J=8 Hz, 1 H), 7.67 (d, J=9 Hz, 1 H), 7.03 (d, J=9 Hz, 1 H), 4.31 (q, J=7 Hz, 2 H), 1.32 (t, J=7 Hz, 3 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07399780B2
Source datasetuspto-grants-2008_07
ORD IDord-51f10148c2b244578cb1b35431e2799d
Source noteuspto-grants-2008_07