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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 579199Generated: October 30, 2026

Sodium triacetoxyborohydride → HCID 86684772, compound

https://huagongshe.com/reaction/579199

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant3-Fluoro-2-(morpholin-4-yl)benzaldehydeHCID 26188751—
ReactantHCID 66684918HCID 66684918—
SolventAcetic AcidHCID 176—
SolventMethanolHCID 887—
ProductHCID 86684772HCID 8668477212%

Reaction Conditions

Temperature75 °C

Reaction Steps

A solution of 3-((R)-2-cyclohexyl-6-oxo-piperazin-1-yl)-5-phenyl-thiophene-2-carboxylic acid (50.0 mg, 0.13 mmol, 1.0 equiv) and 3-fluoro-2-morpholinobenzaldehyde (108.8 mg, 0.52 mmol, 4.0 equiv) in acetic acid (0.2 mL) and methanol (0.5 mL) was stirred at room temperature for 60 minutes. Then sodium triacetoxyborohydride (110.2 mg, 0.52 mmol, 4.0 equiv) was added to the mixture and the resulting mixture was stirred at 75° C. for 3 hours. The solvent was removed by Genevac and the residue was dissolved in EtOAc (6 mL). The organic phase was washed by brine (3 mL), dried over Na2SO4 and concentrated. The residue was purified by HPLC (0.1% NH4OH) to afford the product (9 mg, 12%). MS: 577.2 [M−H+].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09040690B2
Source datasetuspto-grants-2015_05
ORD IDord-48ae17ee13b5499cb2437c6f9cf4d8f0
Source noteuspto-grants-2015_05