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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1189434Generated: November 1, 2026

Nitrogen → 2-Methyl-5-m-tolyl-oxazole-4-carboxylic acid [2-(5-oxo-hexyl)-oxazol-4-yl]-amide

https://huagongshe.com/reaction/1189434

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitrogenHCID 947—
ReactantTrifluoroacetic acidHCID 6422—
Reactant(2-Methyl-5-m-tolyl-oxazole-4-carbonyl)-[2-(5-oxo-hexyl)-oxazol-4-yl]-carbamic acid tert-butyl esterHCID 67128523—
SolventDichloromethaneHCID 6344—
Product2-Methyl-5-m-tolyl-oxazole-4-carboxylic acid [2-(5-oxo-hexyl)-oxazol-4-yl]-amideHCID 49839891—

Reaction Steps

In a flame dried round-bottomed flask equipped with a magnetic stir bar and under inert atmosphere (N2), a solution of (2-methyl-5-m-tolyl-oxazole-4-carbonyl)-[2-(5-oxo-hexyl)-oxazol-4-yl]-carbamic acid tert-butyl ester (50 mg, 0.10 mmol) in dry CH2Cl2 (1.0 mL) was treated at 0° C. with trifluoroacetic acid (0.08 mL, 1.07 mmol). After stirring at rt for 16 h, the reaction mixture was quenched with sat. aq. NaHCO3, extracted with CH2Cl2 (3×10 mL) and the combined org. extracts were dried over Na2SO4, filtered, and the solvents were removed under reduced pressure. Purification of the residue by HPLC gave the title compound as a colorless oil. TLC: rf (6:4 hept-EA)=0.26. LC-MS-conditions 02: tR=1.08 min, [M+H]+=382.50.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08674111B2
Source datasetuspto-grants-2014_03
ORD IDord-d78d3475f9f34815a9e6016b4802feec
Source noteuspto-grants-2014_03