Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | HCID 67438147 | HCID 67438147 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 51348672 | HCID 51348672 | 95.9% |
Reaction Steps
A solution of ((1S,2S)-1-{[(4′-isopropoxy-biphenyl-4-yl)-(2-pyridin-2-yl-cyclopropanecarbonyl)-amino]-methyl}-2-methyl-butyl)-carbamic acid tert-butyl ester (48 mg, 0.084 mmol) and dichloromethane (4 mL) was treated with a solution of HCl in dioxane (4 N, 0.5 mL) and the resulting reaction mixture was maintained at room temperature for 12 h. The reaction was then concentrated to dryness to afford (1R,2R)-2-pyridin-2-yl-cyclopropanecarboxylic acid ((2S,3S)-2-amino-3-methyl-pentyl)-(4′-isopropoxy-biphenyl-4-yl)-amide (38 mg, 95% yield) as a white solid: 1H NMR (400 MHz, MeOD) δ 8.34 (d, J=5.3 Hz, 1H), 7.95 (t, J=7.6 Hz, 1H), 7.55 (d, J=8.1 Hz, 2H), 7.38-7.45 (m, 3H), 7.29-7.37 (m, 3H), 6.88 (d, J=8.6 Hz, 2H), 4.54 (dt, J=12.1, 6.1 Hz, 1H), 4.22 (dd, J=15.0, 9.0 Hz, 1H), 3.65 (dd, J=15.0, 2.7 Hz, 1H), 3.23-3.30 (m, 1H), 2.66-2.76 (m, 1H), 1.99-2.06 (m, 1H), 1.72-1.80 (m, 1H), 1.63-1.71 (m, 1H), 1.45-1.54 (m, 1H), 1.26-1.36 (m, 1H), 1.24 (d, J=6.1 Hz, 6H), 1.05-1.17 (m, 1H), 0.88 (d, J=6.8 Hz, 3H), 0.75 (t, 3H); LRMS (ESI) m/e 472.3 [(M+H)+, calcd for C30H38N3O2 472.3].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08426414B2 |
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| Source dataset | uspto-grants-2013_04 |
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| ORD ID | ord-d2823190b43747cbacd939a4598a508f |
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| Source note | uspto-grants-2013_04 |
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