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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2402015Generated: October 29, 2026

4-Pyridinecarbothioamide → HCID 66747606, compound

https://huagongshe.com/reaction/2402015

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-PyridinecarbothioamideHCID 2723788—
ReactantHCID 86667468HCID 86667468—
SolventIsopropanolHCID 3776—
ProductHCID 66747606HCID 6674760636%

Reaction Steps

To a solution of ethyl 2-chloro-4-(4-chlorophenyl)-3-oxobutanoate (70.8 g, 257 mmol) in IPA (2.96 L) was added thioisonicotinamide (71.1 g, 515 mmol) and the resulting mixture was refluxed for 3 days. The reaction was cooled and concentrated in vacuo and the residue was partitioned between DCM (300 ml) and saturated sodium bicarbonate solution (200 mL). The layers were separated and the aqueous layer was extracted with DCM (100 mL). The combined DCM layers were washed with brine (100 mL), dried over MgSO4, filtered, and concentrated in vacuo to give crude product which was purified by silica gel chromatography (ethyl acetate/DCM=0/100→40/60) followed by recrystallization from ethyl acetate/hexanes to give 33 g of the title compound as yellow crystals. (36% yield). LC/MS (FA) ES+ 359. 1H NMR (400 MHz, CDCl3) δ: 8.74-8.72 (m, 2H), 7.81-7.80 (m, 2H), 7.36-7.32 (m, 2H), 7.27-7.23 (m, 2H), 4.54 (s, 2H), 4.38 (q, 2H, J=7.2 Hz), 1.40 (t, 3H, J=7.2 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08796271B2
Source datasetuspto-grants-2014_08
ORD IDord-8b886c51b5f8467ab25a9d1a659d2925
Source noteuspto-grants-2014_08