HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → 1H-Indazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | 1-Aminopyrrole | HCID 136589 | — |
| Reactant | HCID 178520025 | HCID 178520025 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 1H-Indazole | HCID 9221 | 200.9% |
Reaction Steps
A solution of 6-pyridin-4-yl-1-(2-trimethylsilanyl)-ethoxymethyl)-1H-indazole-3-carbaldehyde (208 mg, 0.59 mmol), N-aminopyrrole (145 mg, 1.76 mmol), and acetic acid (5.8 μl) in ethanol (1 ml) was held at 95° C. for 16 h. The solution was then evaporated under reduced pressure, and purified by silica gel chromatography to give 1H-indazole as an oil (140 mg, 57%). 1H NMR (300 MHz, CDCl3) 9.08 (s, 1H), 8.71 (d, 2H, J=6.1 Hz), 8.46 (d, 1H, J=85 Hz), 834 (s, 1H), 7.85 (d, 2H, J=6.2 Hz), 7.80 (d, 1H, J=8.5 Hz), 7.56 (t, 2H, J=23 Hz), 6.25 (t, 2H, J=2.3 Hz), 5.93 (s, 1H), 5.74 (s, 2H), 3.64 (t, 2H, J=7.9 Hz), 0.86 (t, 2H, J=7.9 Hz), 0.00 (s, 9H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06891044B2 |
| Source dataset | uspto-grants-2005_05 |
| ORD ID | ord-724e9fe38a1b4c33ab564da5f6a31de4 |
| Source note | uspto-grants-2005_05 |