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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1362684Generated: October 30, 2026

Sodium borohydride → HCID 59170971, compound

https://huagongshe.com/reaction/1362684

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 59170865HCID 59170865—
SolventEthanolHCID 702—
ProductHCID 59170971HCID 5917097110.5%

Reaction Steps

Sodium borohydride (2 mg) is added to an ethanol (1 mL) solution of (E)-3-(3-formyl-4-(1H-imidazol-1-yl)phenyl)-N-indan-1-ylacrylamide (17 mg) obtained in Example 437 and the reaction mixture was agitated for 30 minutes at room temperature. After the reaction solution was concentrated under reduced pressure, water and ethyl acetate were added to the residue, and the organic layer was partitioned. The organic layer was washed with a saturated saline solution, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (Carrier: Chromatorex™ NH, elution solvent: methanol-ethyl acetate system), and 1.8 mg of the title compound was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07880009B2
Source datasetuspto-grants-2011_02
ORD IDord-da49a258c8d24f84a416660087976e4c
Source noteuspto-grants-2011_02