Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanolamine | HCID 700 | — |
| Reactant | 4-Methylmorpholine | HCID 7972 | — |
| Reactant | Benzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphate | HCID 151348 | — |
| Reactant | HCID 67171061 | HCID 67171061 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 67172602 | HCID 67172602 | 29.6% |
Reaction Steps
To 2-hydroxy-2-(3-(5-phenyl-4-(trifluoromethyl)isoxazol-3-yl)-4,5-dihydronaphtho[1,2-c]isoxazol-7-yl)propanoic acid (Preparation 134D, isomer 1, 15 mg, 0.032 mmol) in DMF (1 mL) was added 2-aminoethanol (2.9 mg, 0.048 mmol), BOP (18.3 mg, 0.041 mmol) and 4-methylmorpholine (12.9 mg, 0.13 mmol). The reaction mixture was stirred for 1 h. Methanol was added and it was purified by prep HPLC (Phenomenex Luna 5 u 21.2×100 mm, Solvent A: 90% water with 10% acetonitrile and 0.1% TFA, Solvent B: 90% acetonitrile with 10% water and 0.1% TFA, Gradient: 0% B to 100% B over 10 min, 20 mL/min, 220 nM) to yield 2-hydroxy-N-(2-hydroxyethyl)-2-(3-(5-phenyl-4-(trifluoromethyl)isoxazol-3-yl)-4,5-dihydronaphtho[1,2-c]isoxazol-7-yl)propanamide (5 mg, 9.45 μmol, 29.6% yield): product HPLC ret. time=9.07 min (condition G); LC/MS M+1=514.16; 1H NMR (400 MHz, CD3OD) δ ppm 7.91 (1H, d, J=7.92 Hz), 7.77 (2H, d, J=7.26 Hz), 7.58-7.71 (5H, m), 3.60 (2H, td, J=5.72, 3.30 Hz), 3.33-3.41 (2H, m), 3.07 (4H, s), 1.78 (3H, s).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09216972B2 |
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| Source dataset | uspto-grants-2015_12 |
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| ORD ID | ord-4829d323b7774f5d9fbc49e56218fa63 |
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| Source note | uspto-grants-2015_12 |
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