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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2250661Generated: November 2, 2026

Borohydride → HCID 86597482, compound

https://huagongshe.com/reaction/2250661

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBorohydrideHCID 28123—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 86597483HCID 86597483—
SolventEthanolHCID 702—
ProductHCID 86597482HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07317009B2
Source datasetuspto-grants-2008_01
ORD IDord-6036234880044cf3a52830389cb66e19
Source noteuspto-grants-2008_01