HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 707277Generated: October 29, 2026
Triphenylphosphine → HCID 178454106, compound
https://huagongshe.com/reaction/707277
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Diisopropyl diazene-1,2-dicarboxylate | HCID 75555 | — |
| Reactant | 1-Cyclopropyl-1H-imidazo[4,5-b]pyridin-2(3H)-one | HCID 18334875 | — |
| Reactant | HCID 178454125 | HCID 178454125 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178454106 | HCID 178454106 | — |
Reaction Steps
To a solution of tert-butyl(cis-3-hydroxycyclobutyl)carbamate (Intermediate 71) (0.502 g, 2.68 mmol), triphenylphosphine (Sigma-Aldrich, 0.932 ml, 4.02 mmol), 1-cyclopropyl-1H-imidazo[4,5-b]pyridin-2(3H)-one (0.47 g, 2.68 mmol) in THF (10.73 ml) cooled to 0° C. was added diisopropyl azodicarboxylate (Sigma-Aldrich, 0.791 ml, 4.02 mmol) dropwise. The ice bath was removed after 1 h of stirring to allow the mixture to warm to room temperature. After an additional 3 h stirring, the reaction mixture was diluted with EtOAc and washed with saturated NaHCO3 solution. The organic layer was directly loaded onto a Biotage samplet. Purification (0-100% EtOAc/hexane) produced the title compound that solidified upon drying, which was advanced to next step directly without further purification. M+1: 345.0.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09174992B2 |
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| Source dataset | uspto-grants-2015_11 |
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| ORD ID | ord-790017886ffb45108575169cdc3c9257 |
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| Source note | uspto-grants-2015_11 |
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