HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2402015Generated: October 29, 2026
4-Pyridinecarbothioamide → HCID 66747606, compound
https://huagongshe.com/reaction/2402015
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Pyridinecarbothioamide | HCID 2723788 | — |
| Reactant | HCID 86667468 | HCID 86667468 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | HCID 66747606 | HCID 66747606 | 36% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08796271B2 |
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| Source dataset | uspto-grants-2014_08 |
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| ORD ID | ord-8b886c51b5f8467ab25a9d1a659d2925 |
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| Source note | uspto-grants-2014_08 |
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