Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 3,5-Heptanedione | HCID 81923 | — |
| Reactant | HCID 178508400 | HCID 178508400 | — |
| Product | HCID 86719324 | HCID 86719324 | — |
Reaction Steps
A mixture of 3,5-heptanedione (18.8 mg, 0.147 mmol), 2-{[3-(5-amino-1H-1,2,4-triazol-3-yl)propyl](4-fluorophenyl)amino}ethan-1-ol (50 mg, 0.179 mmol), and glacial acetic acid (1 mL) was added to a 50 mL RBF with a magnetic stirring bar. The flask was fitted with a condenser, and warmed in an oil bath to a gentle reflux at 135° C. for 18 h. Progress of the reaction was monitored by analytical HPLC with UV detection (Rt=5.5 min). The mixture was added to stirring ice/water (15 mL), and the pH was adjusted to basic with 1 N sodium hydroxide. The aqueous layer was extracted with ethyl acetate (2×20 mL). The combined organic layers were dried (Na2SO4), filtered and concentrated under reduced pressure. The crude material was purified by silica gel chromatography using a gradient elution of 65-100% ethyl acetate in hexanes. The material was concentrated under reduced pressure and the title compound was obtained (20 mg, 37%). EM (calc.): 413.2; MS (ESI) m/e: 414.2 (M+H)+. 1H NMR (DMSO-d6, 400 MHz) δ ppm: 7.11 (s, 1H), 6.97 (m, 2H), 6.75 (m, 2H), 4.12 (t, 2H), 3.54 (t, 2H), 3.40 (t, 2H), 3.10 (q, 2H), 2.88 (m, 4H), 1.99 (m, 2H), 1.95 (s, 3H), 1.35 (t, 3H), 1.28 (t, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09163027B2 |
|---|
| Source dataset | uspto-grants-2015_10 |
|---|
| ORD ID | ord-80f66516303640c1ab7320b14779bb82 |
|---|
| Source note | uspto-grants-2015_10 |
|---|