HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methylamine → HCID 66693763, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methylamine | HCID 6329 | — |
| Reactant | Glycolaldehyde dimer | HCID 186078 | — |
| Reactant | 1-[Isocyano(4-methylbenzene-1-sulfonyl)methyl]-2-methoxybenzene | HCID 2771653 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 66693763 | HCID 66693763 | 56.8% |
Reaction Steps
To a soln. of 1,4-dioxane-2,5-diol (120 mg, 0.995 mmol) in THF (8 ml) was added methylamine (2.8 ml, 0.664 mmol) at r.t. The resulting mixture was stirred at r.t for 75 min. Then 1-(isocyano(tosyl)methyl)-2-methoxybenzene (200 mg, 0.664 mmol) was added while keeping reaction mixture at <30° C. by a water bath. The reaction mixture was stirred at r.t overnight. Evaporated to leave white solid, dissolved in DMF, and purified by Pre-HPLC to afford (4-(2-methoxyphenyl)-1-methyl-1H-imidazol-5-yl)methanol (84 mg, 0.377 mmol, 38.6% yield) as a colorless oil. 1H-NMR (MeOD), δ: 8.97 (1H, s), 7.55 (1H, t, J=7.5 Hz), 7.47 (1H, d, J=8.0 Hz), 7.22 (1H, d, 8.0 Hz), 7.15 (1H, t, J=7.5 Hz), 4.67 (2H, s), 4.05 (3H, s), 3.89 (3H, s).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08362004B2 |
| Source dataset | uspto-grants-2013_01 |
| ORD ID | ord-0834d909f16a4ab8a73428b1e5da29e2 |
| Source note | uspto-grants-2013_01 |