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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1526283Generated: November 4, 2026

Formic Acid → HCID 117770270, compound

https://huagongshe.com/reaction/1526283

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormic AcidHCID 284—
ReactantAcetic AnhydrideHCID 7918—
ReactantHCID 115938202HCID 115938202—
SolventTetrahydrofuranHCID 8028—
ProductHCID 117770270HCID 117770270—

Reaction Conditions

Temperature55 °C

Reaction Steps

To acetic anhydride (0.703 mL) was added dropwise formic acid (0.349 mL) under ice-cooling, and the mixture was stirred at 55° C. for 45 min. The mixture was allowed to be cooled to room temperature, and tetrahydrofuran (10 mL) was added thereto. A solution of 1-(6-bromopyridin-2-yl)-N-(2,4-dimethoxybenzyl)methanamine obtained in Reference Example 19 (930 mg) in tetrahydrofuran (10 mL) was added dropwise thereto over 3 min under ice-cooling, and the reaction mixture was stirred at room temperature for 30 min. The reaction solution was concentrated under reduced pressure, the obtained colorless oil was subjected to azeotropy with toluene, and the residue was purified by silica gel column chromatography (hexane/ethyl acetate) to give the title compound (932 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09085578B2
Source datasetuspto-grants-2015_07
ORD IDord-7549e05cf34649d488bbfa35aee2ab37
Source noteuspto-grants-2015_07