Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 74280Generated: October 30, 2026

Methanol → 5-(Benzoxazol-2-yl)-2-methyl-1-(3-(morpholin-4-yl)-n-propyl)benzimidazole

https://huagongshe.com/reaction/74280

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantDiethyl EtherHCID 3283—
ReactantSodium BicarbonateHCID 516892—
ReactantEthanimidic acid, methyl ester, hydrochloride (1:1)HCID 10313100—
Reactant2-(N-(2-(morpholin-4-yl)-n-propyl)-2-nitroanilin-4-yl)benzoxazoleHCID 67498563—
Product5-(Benzoxazol-2-yl)-2-methyl-1-(3-(morpholin-4-yl)-n-propyl)benzimidazoleHCID 6749844961%

Reaction Steps

To a solution of 2-(2-(3-(morpholin-4-yl)-n-propyl)aminoanilin-4-yl)benzoxazole (see Working Example 96-1) (300 mg, 0.851 mmol) in methanol (5 mL) was added methyl acetimidate hydrochloride (103 mg, 0.936 mmol), and this was heated to reflux for 3 hours. After the reaction was complete, saturated aqueous sodium hydrogen carbonate solution was added, and this was extracted with ethyl acetate. After the organic layer obtained was dried over anhydrous sodium sulfate, it was filtered and concentrated. To the crystals obtained was added diethyl ether, this was filtered, washed with diethyl ether, and dried to yield the title compound (195 mg, 61% yield) as light brown crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08829035B2
Source datasetuspto-grants-2014_09
ORD IDord-e4c8259744514d4c816fc342c2a97742
Source noteuspto-grants-2014_09