Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Ethyl 1-{2-[3-(2-{3-cyano-4-[(1-methylethyl)oxy]phenyl}-1,3-thiazol-5-yl)-2-ethylphenyl]ethyl}-4-piperidinecarboxylate | HCID 66981746 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | HCID 54576940 | HCID 54576940 | 24.8% |
Reaction Steps
To a solution of ethyl 1-{2-[3-(2-{3-cyano-4-[(1-methylethyl)oxy]phenyl}-1,3-thiazol-5-yl)-2-ethylphenyl]ethyl}-4-piperidinecarboxylate (D86) (204 mg) in isopropanol (40 mL) and water (10 mL) stirred under nitrogen at room temperature was added a solution of NaOH (30.7 mg) in water in one charge. The reaction mixture was stirred at room temperature overnight. Isopropanol was removed in vacuo. The residue was dissolved in water and acidified with 1N HCl to pH=5. The solvent was removed in vacuo, the residue was dissolved in THF, and filtered. The filtrate was purified by Mass Directed AutoPrep to give 1-{2-[3-(2-{3-cyano-4-[(1-methylethyl)oxy]phenyl}-1,3-thiazol-5-yl)-2-ethylphenyl]ethyl}-4-piperidinecarboxylic acid (E37) (48 mg) as a TFA salt (white solid). δH (DMSO-d6, 400 MHz): 1.10 (3H, t), 1.36 (6H, d), 1.76 (2H, m), 2.13 (2H, m), 2.72 (2H, m), 3.07 (4H, m), 3.28 (3H, m), 3.67 (2H, m), 4.91 (1H, m), 7.34 (3H, m), 7.44 (1H, d), 7.85 (1H, s), 8.22 (1H, dd), 8.28 (1H, d), 9.37 (1H, br s), 12.60 (1H, br s). δF (DMSO-d6, 376 MHz): −73.5. MS (ES): C29H33N3O3S requires 503. found 504.1 (M+H+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08389508B2 |
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| Source dataset | uspto-grants-2013_03 |
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| ORD ID | ord-63a06c06f431436991a6f4848b6220b1 |
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| Source note | uspto-grants-2013_03 |
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