HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → HCID 68813830, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 68815476 | HCID 68815476 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 68813830 | HCID 68813830 | — |
Reaction Steps
A solution of [(2-{1-[4-(4,4-Dimethyl-3-oxo-pentyl)-3-isopropyl-phenyl]-1-ethyl-propyl}-benzofuran-5-carbonyl)-methyl-amino]-acetic acid (27 mg, 0.05 mmol) (Example 55) in THF (2 mL) is treated with NaBH4 (4 mg, 0.1 mmol) at room temp. The resulting mixture is stirred for 2 hours. The mixture is concentrated and neutralized to pH 3 and extracted with EtOAc (3×5 mL). The organic layer is dried over sodium sulfate, concentrated to afford the desired compound. (17 mg, 63%) MS (ES) m/e: 536.3 (M−1)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07579488B2 |
| Source dataset | uspto-grants-2009_08 |
| ORD ID | ord-8f37f8c73f524e0eaebd801191131617 |
| Source note | uspto-grants-2009_08 |