HuagongsheHuagongshe Chemistry Print Report · For research reference only
Borohydride → HCID 86597482, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Borohydride | HCID 28123 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 86597483 | HCID 86597483 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 86597482 | HCID 86597482 | — |
Reaction Steps
To a solution of 5-[4-(2-chloro-4-pyridinyl)-7-ethyl-2-methylpyrrolo[1,2-b]pyridazin-3-yl]-5-oxopentanoic acid (47 mg) in EtOH (1 mL) was added sodium borohydride (5 mg) in an ice-water bath under N2. After 10 min, the mixture was stirred at ambient temperature. After 1 h, another odium borohydride (5 mg) was added. After 2 h, the reaction mixture was partitioned between CHCl3 and H2O. The aqueous layer was extracted with CHCl3 twice. The combined organic layer was dried over MgSO4 and evaporated in vacuo. The residue was purified by p-TLC (CHCl3-MeOH=10-1) to give 5-[4-(2-chloro-4-pyridinyl)-7-ethyl-2-methylpyrrolo[1,2-b]pyridazin-3-yl]-5-hydroxypentanoic acid as yellow amorphous (28 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07317009B2 |
| Source dataset | uspto-grants-2008_01 |
| ORD ID | ord-6036234880044cf3a52830389cb66e19 |
| Source note | uspto-grants-2008_01 |