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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 74229Generated: October 29, 2026

Trimethyl orthoacetate → 5-(Benzoxazol-2-yl)-2-methyl-1-cyclopropylmethylbenzimidazole

https://huagongshe.com/reaction/74229

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethyl orthoacetateHCID 15050—
ReactantHCID 67498091HCID 67498091—
SolventMethanolHCID 887—
Product5-(Benzoxazol-2-yl)-2-methyl-1-cyclopropylmethylbenzimidazoleHCID 6749809263.5%

Reaction Steps

To a methanol (5 mL) solution of 2-(2-cyclopropylmethylaminoanilin-5-yl)benzoxazole (see Working Example 54-1) (140 mg, 0.425 mmol) was added 1,1,1-trimethoxyethane (75 mg, 0.624 mmol), and this was stirred at room temperature for 10 hours. After the reaction was complete, this was concentrated, and the residue obtained was purified by silica gel column chromatography to yield the title compound (81.9 mg, 54% yield) as pink crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08829035B2
Source datasetuspto-grants-2014_09
ORD IDord-34159f691ed3462a99625c552f00d970
Source noteuspto-grants-2014_09