HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2170746Generated: October 30, 2026
Triphenylphosphine → HCID 178453991, compound
https://huagongshe.com/reaction/2170746
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 5-bromo-1H-indazole | HCID 761929 | — |
| Reactant | Diisopropyl azodicarboxylate | HCID 5363146 | — |
| Reactant | HCID 178418329 | HCID 178418329 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178453991 | HCID 178453991 | — |
Reaction Steps
A solution of 5-bromoindazole (15 g), tert-butyl trans-4-hydroxycyclohexylcarbamate (50 g) and triphenylphosphine (50 g) in THF was stirred at 0° C. for 15 minutes. To the reaction solution was added dropwise diisopropylazodicarboxylate (38.5 g) under nitrogen atmosphere at 0° C., and the mixture was stirred at 50° C. for 1 day. Then, the solvent was removed out, ethyl acetate (300 mL) and petroleum ether (90 mL) were added thereto, and the mixture was stirred at room temperature for 2 hours. The reaction solution was filtered, the solvent was evaporated under reduced pressure, and the residue was purified by silica gel column chromatography (ethyl acetate:petroleum ether=1:80-1:15 as the eluting solvent) to give Compound Q11 (8.00 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09051295B2 |
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| Source dataset | uspto-grants-2015_06 |
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| ORD ID | ord-c6d48e549d53400da7516faea607c3bb |
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| Source note | uspto-grants-2015_06 |
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