HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → Merck SIP Agonist
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | 3-azetidinecarboxylic Acid | HCID 93192 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | [4-[5-[4-(2-Methylpropyl)phenyl]-1,2,4-oxadiazol-3-yl]phenyl]methanol | HCID 11645224 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Merck SIP Agonist | HCID 10430549 | 74% |
Reaction Steps
A solution of 3.06 g (10.0 mmol) of Aldehyde 1, 1.06 g (10.5 mmol) of 3-azetidine carboxylic acid and 5 mL of acetic acid in 150 mL of methanol was stirred for 20 min at rt. A solution of sodium cyanoborohydride (380 mg, 5.0 mmol) in 20 mL of methanol was added. The reaction mixture was stirred for 1 h then was filtered. The solids were washed with 30 ml of methanol and dried to afford 2.88 g (74%) of the title compound: 1H NMR (400 Mhz, CD3OD) δ 0.95 (d, J=6.6, 6H), 1.96 (m, 1H), 2.62 (d, J=7.3, 2H), 3.42 (m, 1H), 4.19 (m, 4H), 4.41 (s, 2H), 7.43 (d, J=8.0, 2H), 7.64 (d, J=8.2, 2H), 8.14 (d, J=8.0, 2H), 8.23 (d, J=8.2, 2H); ESI-MS 392 (M+H); LC-1: 3.0 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07199142B2 |
| Source dataset | uspto-grants-2007_04 |
| ORD ID | ord-fbe47b1e6b884ac697340a2fc5989673 |
| Source note | uspto-grants-2007_04 |