HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triphenylphosphine → 3((1-BOC-2-(S)-pyrrolidinyl)methoxy)-5-trifluoromethylpyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Diethyl azodicarboxylate | HCID 5462977 | — |
| Reactant | tert-butyl (2S)-2-(hydroxymethyl)azetidine-1-carboxylate | HCID 10511797 | — |
| Reactant | 5-(Trifluoromethyl)pyridin-3-ol | HCID 22989707 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3((1-BOC-2-(S)-pyrrolidinyl)methoxy)-5-trifluoromethylpyridine | HCID 21309665 | — |
Reaction Steps
A 333 mg (1.20 mmol) sample of 1-BOC-2-(S)-azetidinemethanol, prepared as in Example 7b above, and 230 mg (1.30 mmol) of 3-hydroxy-5-trifluoromethylpyridine, from step 66b above, were reacted with triphenylphosphine and DEAD (1.2 mmol each) in 5 mL of THF according to the procedure of Example 14a, to give 360 mg of the title compound. MS (D)CI/NH3) m/e 347 (M+H)+. 1H so NMR (CDCl3, 300 MHz) δ: 8.50 (s, 1H), 8.48 (s, 1H), 7.46 (s, 1H), 4.28-3.90 (m, 3H), 3.48-3.84 (m, 2H), 2.12-1.87 (m, 4H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05914328 |
| Source dataset | uspto-grants-1999_06 |
| ORD ID | ord-c5e027c3dec9468da59c43a29757ac20 |
| Source note | uspto-grants-1999_06 |