HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Azido-4-fluorobenzene → (S)-tert-Butyl 2-(4-(1-(4-fluorophenyl)-1H-1,2,3-triazol-4-yl)phenyl)morpholine-4-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Azido-4-fluorobenzene | HCID 10887974 | — |
| Reactant | (S)-tert-butyl 2-(4-ethynylphenyl)morpholine-4-carboxylate | HCID 89689402 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Solvent | Diisopropylethylamine | HCID 81531 | — |
| Product | (S)-tert-Butyl 2-(4-(1-(4-fluorophenyl)-1H-1,2,3-triazol-4-yl)phenyl)morpholine-4-carboxylate | HCID 118412982 | 28.4% |
Reaction Steps
1-Azido-4-fluorobenzene (24 mg, 0.174 mmol) was dissolved in N,N-diisopropylethylamine (0.75 ml), then (S)-tert-butyl 2-(4-ethynylphenyl)morpholine-4-carboxylate (50 mg, 0.175 mmol) was added followed by copper(I) iodide (33 mg, 0.174 mmol). The mixture was stirred at room temperature for 3 h. The green mixture was concentrated on the rotavap, silica gel (0.5 g) was added and after short grinding the mixture was put on a silica gel column for purification. Flash chromatography (5 g silica gel, 30% ethyl acetate in heptane) yielded a white solid (21 mg, 28%). MS (ISP): 369.1 ([M-tBu+H]+), 425.2 ([M+H]+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09181230B2 |
| Source dataset | uspto-grants-2015_11 |
| ORD ID | ord-60a29c3938d6495ba2ccafdd9d507156 |
| Source note | uspto-grants-2015_11 |