HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 748521Generated: October 28, 2026
Sodium hydride → HCID 136342113, compound
https://huagongshe.com/reaction/748521
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 5-Nitro-2-oxindole | HCID 230366 | — |
| Reactant | Ethyl 6-chloronicotinate | HCID 2799611 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ammonium Chloride | HCID 25517 | — |
| Solvent | Dimethylazanide | HCID 182180 | — |
| Product | HCID 136342113 | HCID 136342113 | 47% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07399780B2 |
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| Source dataset | uspto-grants-2008_07 |
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| ORD ID | ord-51f10148c2b244578cb1b35431e2799d |
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| Source note | uspto-grants-2008_07 |
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