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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1945483Generated: November 3, 2026

1,2-Dichloroethane → Benzoxazole-6-carboxylic acid (furan-2-ylmethyl)-amide

https://huagongshe.com/reaction/1945483

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
ReactantFurfurylamineHCID 3438—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantDiisopropylethylamineHCID 81531—
Reactant2-(4-Adamantan-1-yl-phenoxymethyl)-benzoxazole-6-carboxylic acidHCID 24966535—
Solvent2,4,6-Tris((dimethylamino)methyl)phenolHCID 7026—
ProductBenzoxazole-6-carboxylic acid (furan-2-ylmethyl)-amideHCID 8663708432.5%

Reaction Steps

To solution of 2-(4-adamantan-1-yl-phenoxymethyl)-benzoxazole-6-carboxylic acid (30.1 mg, 0.08 mmol), furfuryl amine (11.0 mg, 0.12 mmol, 0.01 ml), EDC (21.7 mg, 0.12 mmol) and HOBt (15.4 mg, 0.12 mmol) in DMF 3.0 mL was added DIPEA (14.2 mg, 0.12 mmol, 0.02 ml). After stirring at room temperature, the mixture was partitioned between ethyl acetate and brine. The organic phase was dried (MgSO4 anh), and concentrated. The residue was purified by silica gel column chromatography (n-Hexane:EtOAc:MeOH=6:3:1) to give 2-adamantan-1-yl-phenoxymethyl)-benzoxazole-6-carboxylic acid (furan-2-ylmethyl)-amide as a white solid (6.3 mg, 17.4% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08394799B2
Source datasetuspto-grants-2013_03
ORD IDord-badc8e4ce7444289949d5fc6eaeed883
Source noteuspto-grants-2013_03