HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 86690813, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Isonicotinoyl chloride hydrochloride | HCID 12262826 | — |
| Reactant | HCID 86690811 | HCID 86690811 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 86690813 | HCID 86690813 | 78% |
Reaction Steps
To a solution of 4-(4-(dimethylamino)-2,6-dimethylphenyl)thiazol-2-amine (1-4, 0.50 g, 2.0 mmol) in CH2Cl2 (5.1 mL) was added triethylamine (0.61 g, 6.1 mmol) followed by isonicotinoyl chloride hydrochloride (0.54 g, 3.0 mmol). The reaction mixture was stirred at room temperature overnight. The solution was concentrated under reduced pressure and added with hot water. The resultant precipitate was filtered and dried under vacuum to give N-{4-(4-(dimethylamino)-2,6-dimethylphenyl)thiazol-2-yl}isonicotinamide (1, 0.55 g) as yellow solids in 77% yield: 1H NMR (500 MHz, CDCl3) δ 8.64 (d, J=5.5 Hz, 2 H), 7.55 (d, J=5.5 Hz, 2 H), 6.74 (s, 1 H), 6.12 (s, 2 H), 2.89 (s, 6 H), 1.91 (s, 6 H). ESI-MS: m/z 352.6 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08999983B2 |
| Source dataset | uspto-grants-2015_04 |
| ORD ID | ord-26aa8ca8a2c647acabff6a3eb152f4ec |
| Source note | uspto-grants-2015_04 |