Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Aniline | HCID 6115 | — |
| Reactant | PyBroP | HCID 2733179 | — |
| Reactant | HCID 66934634 | HCID 66934634 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | Methanol--water (1/1) | HCID 22242641 | — |
| Product | HCID 66934465 | HCID 66934465 | 58% |
Reaction Steps
(S)-3-(5-chloropyridin-2-yl)-3-(3-fluoro-5-(trifluoromethyl)phenyl)-3-pivalamidopropanoic acid (0.10 g, 0.21 mmol) was dissolved in MeOH (2 mL) and 4M HCl in dioxanes added (2 mL). The resulting solution was stirred at RT for 30 mins then the solvents were removed under reduced pressure yielding a pale yellow oil (crude quantative) LCMS: 1.31 min [M+1] 363.2 (2 min gradient, MeOH/H2O 0.1% TFA). The residue was dissolved in acetonitrile (5 mL) and TEA, (0.3 mL, excess), aniline (0.030 g, 0.32 mmol) and PyBrOP (0.11 g, 0.24 mmol) added at RT. The RM was stirred for 14 h, concentrated to 1.5 mL, filtered and purified by prep HPLC: YMC ODSA30×100 mm, 40ml/min, 20-100% MeOH (0.1% TFA) over 10 min. The product (S)-3-amino-3-(5-chloropyridin-2-yl)-3-(3-fluoro-5-(trifluoromethyl)phenyl)-N-phenylpropanamide with a retention time of 7.52 min was isolated as a pale yellow oil, (0.054 g, 58% yield). LCMS: 1.48 min [M+1] 438.2 (2 min gradient, MeOH/H2O 0.1% TFA).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07888376B2 |
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| Source dataset | uspto-grants-2011_02 |
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| ORD ID | ord-6640dede3ac64167ad42dc9fe066e5a9 |
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| Source note | uspto-grants-2011_02 |
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