Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | 2,6-Lutidine | HCID 7937 | — |
| Reactant | 1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide | HCID 15908 | — |
| Reactant | HOAt | HCID 181649 | — |
| Reactant | (3R)-3-Amino-4-phenylbutanoic acid--hydrogen chloride (1/1) | HCID 24820568 | — |
| Reactant | HCID 178439323 | HCID 178439323 | — |
| Product | HCID 178439315 | HCID 178439315 | 92% |
Reaction Steps
A solution of 5-propyl-1-[2′-(1H-tetrazol-5-yl)-biphenyl-4-ylmethyl]-1H-pyrazole-3-carboxylic acid (200 mg, 510 μmol), HOAt (77.1 mg, 566.4 μmol), EDCI (108.6 mg, 566.4 μmol), and 2,6-lutidine (357.8 μL, 3.1 mmol) in DCM (6.1 mL, 94.7 mmol) was stirred to pre-activate the acid. After 30 minutes, the mixture was cooled at 0° C. and (R)-3-amino-4-phenylbutyric acid hydrochloride (122.2 mg, 566.4 μmol) was added. The resulting solution was slowly warmed to room temperature and stirred overnight. The mixture was then concentrated, re-dissolved in water/MeCN/TFA and purified using reverse phase liquid chromatography to yield the title compound (59 mg; 92% purity). MS m/z: [M+H]+ calcd for C31H31N7O3, 550.25; found 550.4.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08350027B2 |
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| Source dataset | uspto-grants-2013_01 |
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| ORD ID | ord-1368bae789d44b61a00acde52d1fb102 |
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| Source note | uspto-grants-2013_01 |
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