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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 17325Generated: October 30, 2026

Acetic Acid → HCID 68585790, compound

https://huagongshe.com/reaction/17325

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantFormaldehydeHCID 712—
ReactantSodium CarbonateHCID 10340—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactant2-tert-Butyl-5-methyl-7-(3-methylaminoazetidin-1-yl)-6-phenyl-1,3-benzoxazole-4-carbonitrileHCID 68584000—
SolventMethanolHCID 887—
SolventSodium chloride; waterHCID 57417360—
ProductHCID 68585790HCID 6858579088%

Reaction Conditions

Temperature0 °C

Reaction Steps

Aqueous 36% formaldehyde solution (205 μl, 2.75 mmol) was added to a methanol (4 ml) solution of 2-tert-butyl-5-methyl-7-(3-methylaminoazetidin-1-yl)-6-phenyl-1,3-benzoxazole-4-carbonitrile (I-73) (103 mg, 275 μmol), followed by cooling at 0° C. Sodium cyanoborohydride (34.6 mg, 550 μmol) and acetic acid (40.9 μl, 715 μmol) were added, followed by stirring at room temperature for 20 minutes. Aqueous 10% sodium carbonate solution and saturated brine were added to the reaction liquid, and this was extracted with ethyl acetate and chloroform. The organic layers were combined, dried over anhydrous magnesium sulfate, concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography (chloroform:methanol=200:1), again purified by silica gel column chromatography (dichloromethane:ethyl acetate=1:1) to obtain the entitled compound (94 mg, 88%) as a colorless solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07737166B2
Source datasetuspto-grants-2010_06
ORD IDord-aa314d9d38e24de0969d47d7dc94b2a9
Source noteuspto-grants-2010_06