HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triphenylphosphine → HCID 86711768, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | N-(tert-Butoxycarbonyl)-N-methyl-2-aminoethanol | HCID 545700 | — |
| Reactant | Diisopropyl azodicarboxylate | HCID 5363146 | — |
| Reactant | 2,4,6-Trichloropyrimidin-5-ol | HCID 86667332 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 86711768 | HCID 86711768 | 124.5% |
Reaction Steps
A mixture of 2,4,6-trichloro-pyrimidin-5-ol (300 mg, 1.50 mmol), (2-hydroxy-ethyl)-methyl-carbamic acid tert-butyl ester (300 mg, 1.71 mmol), triphenylphosphine (455 mg, 1.73 mmol) and DIAD (339 μL, 1.73 mmol) in dioxane (2.5 mL) was stirred at RT for 1.5 hours then concentrated in vacuo. The resulting residue was purified by column chromatography (SiO2, gradient 0-50% ethyl acetate in cyclohexane) affording Methyl-[2-(2,4,6-trichloro-pyrimidin-5-yloxy)-ethyl]-carbamic acid tert-butyl ester (666 mg, quantitative). LCMS: RT=3.09 min, [M-Boc+Na]+=279.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09346817B2 |
| Source dataset | uspto-grants-2016_05 |
| ORD ID | ord-64c81e2704e340908a00980301f7aa4a |
| Source note | uspto-grants-2016_05 |