Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Isonicotinoyl chloride hydrochloride | HCID 12262826 | — |
| Reactant | HCID 86690868 | HCID 86690868 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 86690870 | HCID 86690870 | 27% |
Reaction Steps
To a solution of 4-{4-(4-(3-methoxypropoxy)phenoxy)-2,6-dimethylphenyl}thiazol-2-amine (21-5, 0.28 g, 0.74 mmol) in CH2Cl2 (5.0 mL) was added triethylamine (0.5 mL, 3.59 mmol) followed by isonicotinoyl chloride hydrochloride (0.22 g, 1.22 mmol). The reaction mixture was stirred at room temperature overnight. The solution was concentrated under reduced pressure and added with water. The resultant precipitate was filtered and recrystallized in toluene to give N-{4-(4-(4-(3-methoxypropoxy)phenoxy)-2,6-dimethylphenyl}thiazol-2-yl)isonicotinamide (21, 0.99 mg) as light yellow solids in 27% yield: 1H NMR (500 MHz, DMSO-d6) δ 13.00 (s, 1 H), 8.81 (s, 2 H), 7.99 (d, J=5.7 Hz, 2 H), 7.15 (s, 1 H), 6.98 (m, 4 H), 6.68 (s, 2 H), 4.00 (t, J=6.3 Hz, 2 H), 3.47 (t, J=6.3 Hz, 1 H), 2.05 (s, 6 H), 1.94 (t, J=6.3 Hz, 2 H). ESI-MS: m/z 489.7 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08999983B2 |
|---|
| Source dataset | uspto-grants-2015_04 |
|---|
| ORD ID | ord-fc4288818114476d8300ac8aea0e80e9 |
|---|
| Source note | uspto-grants-2015_04 |
|---|