HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 657589Generated: October 30, 2026
Thionyl Chloride → HCID 57624577, compound
https://huagongshe.com/reaction/657589
Participants
| Role | Name | HCID | Charge |
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| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | HCID 25230624 | HCID 25230624 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 57624577 | HCID 57624577 | — |
Reaction Steps
A solution of 2-[3,5-dichloro-4-(1-hydroxymethyl-5-isopropyl-6-oxo-1,6-dihydro-pyridazin-3-yloxy)-phenyl]-3,5-dioxo-2,3,4,5-tetrahydro-[1,2,4]triazine-6-carbonitrile (600 mg, 1.29 mmol) in tetrahydrofuran (9.0 mL, 0.14 M) cooled to 0° C. was treated with thionyl chloride (0.28 mL, 3.84 mmol). The reaction mixture was allowed to slowly warm to 25° C. The reaction mixture was stirred at 25° C. overnight. At this time, the reaction mixture was concentrated in vacuo. The residue was taken up in benzene and was re-concentrated twice to afford 2-[3,5-dichloro-4-(1-chloromethyl-5-isopropyl-6-oxo-1,6-dihydro-pyridazin-3-yloxy)-phenyl]-3,5-dioxo-2,3,4,5-tetrahydro-[1,2,4]triazine-6-carbonitrile as a yellow solid. The material was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08076334B2 |
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| Source dataset | uspto-grants-2011_12 |
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| ORD ID | ord-b77fc0ea1494458c98c26ff0d3827b33 |
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| Source note | uspto-grants-2011_12 |
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