HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1873982Generated: November 3, 2026
Triphenylphosphine → HCID 59370710, compound
https://huagongshe.com/reaction/1873982
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | N,N-Dibenzylethanolamine | HCID 22657 | — |
| Reactant | Diamide | HCID 5353800 | — |
| Reactant | HCID 135869969 | HCID 135869969 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 59370710 | HCID 59370710 | 88.9% |
Reaction Steps
Tert-butyl 3-chloro-6-hydroxyindazole-1-carboxylate (4.3611 g) which can be prepared according to the method described in Reference example 39, etc. and 2-(dibenzylamino)ethanol (4.1529 g; manufactured by Tokyo Chemical Industry Co., Ltd.) were dissolved in dehydrated THF (100 mL), added with triphenylphosphine (7.9370 g; manufactured by Kanto Chemical Co., Inc.) and TMAD (5.2270 g; manufactured by Masuda Chemical Industries Co., Ltd.), and then stirred overnight at room temperature. The reaction solution was filtered and the filtrate was concentrated under reduced pressure. The resulting residue was dissolved in toluene, and the solvent was evaporated under reduced pressure. The resulting residue was purified by column chromatography (“COLUMN-D”; n-hexane:ethyl acetate=90:10→75:25) to obtain the title compound (7.1028 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08304443B2 |
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| Source dataset | uspto-grants-2012_11 |
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| ORD ID | ord-749e437dbb7a4095aa73970ed5e73eeb |
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| Source note | uspto-grants-2012_11 |
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