HuagongsheHuagongshe Chemistry Print Report · For research reference only
Isopropylethanediol → HCID 86661732, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Isopropylethanediol | HCID 7996 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 86661733 | HCID 86661733 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 86661732 | HCID 86661732 | 45.4% |
Reaction Steps
A mixture of 2,6-dichloro-5-(trifluoromethyl)nicotinamide (0.35 g, 1.35 mmol) and 2-isopropoxyethanol (0.14 g, 1.35 mol) in DMF (20 mL) was added sodium hydride (59 mg, 1.48 mmol) in portions at 0° C. The mixture was stirred at r.t for 2 hrs, quenched by water, extracted by EtOAc and the organic layer was concentrated in vacuo to afford 6-chloro-2-(2-isopropoxyethoxy)-5-(trifluoromethyl)nicotinamide (0.2 g, 45.4%). 1H-NMR (400 MHz, DMSO-d6) δ (ppm) 8.45 (s, 1H), 8.05 (bs, 1H), 7.63 (bs, 1H), 4.54-4.52 (m, 2H), 3.75-3.72 (m, 2H), 3.64-3.58 (m, 1H), 1.07-1.06 (d, 6H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09145429B2 |
| Source dataset | uspto-grants-2015_09 |
| ORD ID | ord-0b8e5fc6dffb456bb0165d524b80413e |
| Source note | uspto-grants-2015_09 |