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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 74274Generated: October 25, 2026

Acetaldehyde → 5-(Benzoxazol-2-yl)-2-methyl-1-tert-butoxycarbonylmethylbenzimidazole

https://huagongshe.com/reaction/74274

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetaldehydeHCID 177—
ReactantPotassium CarbonateHCID 11430—
ReactantPotassium hydroxy sulfiteHCID 23707502—
Reactant2-(2-(Tert-butoxycarbonylmethylamino)anilin-5-yl)benzoxazoleHCID 67498333—
SolventDimethylformamideHCID 6228—
Product5-(Benzoxazol-2-yl)-2-methyl-1-tert-butoxycarbonylmethylbenzimidazoleHCID 6749780524%

Reaction Steps

To a solution of 2-(2-(tert-butoxycarbonylmethylamino)anilin-5-yl)benzoxazole (see Working Example 91-1) (120 mg, 0.353 mmol) in dimethylformamide (2 mL) was added an aqueous solution of acetaldehyde (approx. 90%, 66 μL, 1.06 mmol) and oxone (217 mg, 0.353 mmol), and this was stirred at room temperature for 2 hours. After the reaction was complete, aqueous potassium carbonate solution was added, this was filtered and washed with water. The crystals obtained were purified by silica gel column chromatography to yield the title compound (30.7 mg, 24% yield) as white crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08829035B2
Source datasetuspto-grants-2014_09
ORD IDord-e19a6ef2df6b4adf929f599fe0a11e2c
Source noteuspto-grants-2014_09