HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → HCID 23599483, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 23599482 | HCID 23599482 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 23599483 | HCID 23599483 | 62.1% |
Reaction Steps
To the solution of (R)-N-(1-azabicyclo[2.2.2]oct-3-yl)(5-(3-formylphenyl)thiophene-2-carboxamide) (875 mg) in methanol (15 mL), sodium borohydride (97.2 mg) was added. The mixture was then stirred at room temperature for 4 h. The residue was partitioned between water and chloroform. The extracts were dried over magnesium sulfate, filtered, and evaporated, and the residue was then purified by flash chromatography using 5–20% 3.5M methanolic ammonia/chloroform mixtures as the eluent to give the title compound (547 mg); MS (ES+) 343 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07214688B2 |
| Source dataset | uspto-grants-2007_05 |
| ORD ID | ord-822056e8e1c04ae687f52d7738130b2a |
| Source note | uspto-grants-2007_05 |