HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1520397Generated: November 2, 2026
Triphenylphosphine → HCID 67298266, compound
https://huagongshe.com/reaction/1520397
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Dibenzyl azodicarboxylate | HCID 5387121 | — |
| Reactant | 6-(hydroxymethyl)-3-methyl-2,3-dihydro-1,3-benzoxazol-2-one | HCID 54129573 | — |
| Reactant | HCID 67297993 | HCID 67297993 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 67298266 | HCID 67298266 | — |
Reaction Steps
To 6-(hydroxymethyl)-3-methylbenzo[d]oxazol-2(3H)-one (45.1 μmol) was added the solution of 3-(4-(methylamino)-2-(pyridin-3-yl)quinazolin-6-yl)phenol (30 μmol) in THF (400 μL). After PS-triphenylphosphine (60 μmol) was added, the solution of DBAD (di-tert-butyl azodicarboxylate, 66 mmol) in THF was dispensed to the vials. The mixture was heated at 50° C. for 8 h. After the solvent was removed, the residue was diluted with methanol and purified by Mass triggered PREP-HPLC Condition D. The target fraction was lyophilized to afford the titled compound whose structure was finally confirmed by LCMS using LCMS Method E.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09073890B2 |
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| Source dataset | uspto-grants-2015_07 |
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| ORD ID | ord-17fb77be2ebd484e878d4d688d24980e |
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| Source note | uspto-grants-2015_07 |
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