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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 917716Generated: November 1, 2026

HCID 11403394, compound → HCID 11437715, compound

https://huagongshe.com/reaction/917716

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 11403394HCID 11403394—
CatalystPalladiumHCID 23938—
SolventMeOH tetrahydrofuranHCID 21899815—
ProductHCID 11437715HCID 1143771582%

Reaction Steps

4-(4-Ethynyl-2-fluoroanilino)-1-methyl-6-oxo-1,6-dihydro-3-pyridinecarboxamide was hydrogenated in MeOH/THF in the presence of 5% Pd/C as for example 3. Purification of the crude oil was carried out by column chromatography on silica gel (50% acetone/CH2Cl2 as eluant) to give 4-(4-ethyl-2-fluoroanilino)-1-methyl-6-oxo-1,6-dihydro-3-pyridinecarboxamide as a cream solid (82%), m.p. (EtOAc) 268-272° C. 1H NMR [(CD3)2SO, 400 MHz] δ 10.14 (s, 1H), 8.32 (s, 1H), 7.84 (br s, 1H), 7.43 (br s, 1H), 7.33 (t, J=8.4 Hz, 1H), 7.19 (dd, J=11.1, 1.7 Hz, 1H), 7.08 (dd, J=8.2, 1.5 Hz, 1H), 5.39 (d, J=1.1 Hz, 1H), 3.36 (s, 3H), 2.62 (q, J=7.6 Hz, 2H), 1.19 (t, J=7.6 Hz, 3H). Anal. Calcd for C15H16FN3O2: C, 62.3; H, 5.6; N, 14.5. Found: C, 62.5; H, 5.4; N, 14.8.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07273877B2
Source datasetuspto-grants-2007_09
ORD IDord-008d25876347426d83a786cb5dabc432
Source noteuspto-grants-2007_09