HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1835174Generated: November 3, 2026
Triphenylphosphine → HCID 23503292, compound
https://huagongshe.com/reaction/1835174
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 2,6-Di-tert-butylphenol | HCID 31405 | — |
| Reactant | 2-(Methylthio)ethanol | HCID 78925 | — |
| Reactant | Diethyldiazodicarboxylate | HCID 14357405 | — |
| Reactant | HCID 23503283 | HCID 23503283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 23503292 | HCID 23503292 | — |
Reaction Steps
To 5 ml of dry tetrahydrofuran was added 0.64 ml of 1M triphenylphosphine in tetrahydrofuran followed by 0.64 ml of 1M diethyl diazodicarboxylate in tetrahydrofuran and then by 0.64 ml of 1M 2,6-di-t-butylphenol in tetrahydrofuran. This mixture was mixed for 5 minutes and then 1.28 ml of 0.5M 2-(methylthio)ethanol in tetrahydrofuran was added. The solution was then mixed for 5 minutes. 7-Cyclopropylmethyl-3-hydroxy-5-methyl-2-[(3-trifluoromethylphenyl)methyl]thieno[2,3-d]pyridazin-4(5H)-one (248 mg in 1 ml tetrahydrofuran) was added and the solution was mixed periodically over 24 hours. The solution was opened to the air for 18 hours and then purified by chromatography, eluting with an isohexane ethyl acetate gradient, to give the title compound (77 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06770646B2 |
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| Source dataset | uspto-grants-2004_08 |
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| ORD ID | ord-84826709835f45428f8b068fbb8d49a2 |
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| Source note | uspto-grants-2004_08 |
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