HuagongsheHuagongshe Chemistry Print Report · For research reference only
1H-imidazole-2-carbaldehyde → 2-(2-formyl-1H-imidazol-1-yl)-N-(3-iodophenyl)acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1H-imidazole-2-carbaldehyde | HCID 24955 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 2-bromo-N-(3-iodophenyl)acetamide | HCID 44883470 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-(2-formyl-1H-imidazol-1-yl)-N-(3-iodophenyl)acetamide | HCID 86692722 | 94% |
Reaction Steps
A solution of 2-bromo-N-(3-iodophenyl)acetamide (2.67 g, 7.83 mmol), 1H-imidazole-2-carbaldehyde (0.752 g, 7.83 mmol) and DIPEA (10 mL) in DMF (20 mL) was stirred at 80° C. for 4 hrs. The solvent was evaporated under reduced pressure to afford a residue, which was purified by Biotage eluting with DCM in hexanes to 10% MeOH in DCM to give 2-(2-formyl-1H-imidazol-1-yl)-N-(3-iodophenyl)acetamide (2.60 g, 94%). 1H NMR (400 MHz, DMSO) 9.64 (s, 1H), 8.17 (brs, 1H), 8.04 (s, 1H), 7.60 (s, 1H), 7.46 (d, J=8.4 Hz, 1H), 7.40 (d, J=8.0 Hz, 1H), 7.28 (s, 1H), 7.10 (t, J=8.0 Hz, 1H), 5.23 (s, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09422251B2 |
| Source dataset | uspto-grants-2016_08 |
| ORD ID | ord-8dd05e96cb254a9c94f589c4062202ac |
| Source note | uspto-grants-2016_08 |