HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1521829Generated: October 30, 2026
HCID 66579130, compound → HCID 66581013, compound
https://huagongshe.com/reaction/1521829
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 66579130 | HCID 66579130 | — |
| Catalyst | Iron | HCID 23925 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 66581013 | HCID 66581013 | — |
Reaction Steps
To a solution of ethyl 1-(1-oxidopyridin-3-yl)-1,4-dihydrothiochromeno[4,3-c]pyrazole-3-carboxylate 5,5-dioxide (300 mg, 0.78 mmol) in glacial acetic acid (15 mL) is added iron powder (175 mg, 3.12 mmol). The reaction mass is heated to 85° C. for 1 h under nitrogen. The reaction progress is monitored by TLC. The solvent is removed completely under reduced pressure. The crude material obtained is diluted with water and is extracted with ethylacetate. The organic layer is separated and is dried using sodium sulphate and concentrated under reduced pressure to afford the title compound. 1H NMR (400 MHz, DMSO-d6) δ=8.85-8.84 (d, J=4.7 Hz, 1H), 8.79-8.78 (m, 1H), 8.07-8.03 (m, 2H), 7.70-7.59 (m, 3H), 6.87-6.85 (d, J=7.84 Hz, 1H), 5.00 (s, 2H), 4.40-4.35 (q, 2H), 1.35-1.32 (t, J=7.12 Hz, 3H). MS (ESI+): 370.2. HPLC (max plot): 97.29%; Rt 3.24 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09073940B2 |
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| Source dataset | uspto-grants-2015_07 |
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| ORD ID | ord-f167b4eb10e84642b49e88c8c4c4ee6a |
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| Source note | uspto-grants-2015_07 |
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