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HRID 555903作成日:2026年10月26日

Hydroxide → 4-Chloro-2-{[(2,5-dimethylfuran-3-yl)carbonyl]amino}benzoic acid

https://huagongshe.com/reaction/555903

反応式

関与物質

役割名称HCID仕込み量
反応物HydroxideHCID 961—
反応物N,N-diethyl-m-toluamideHCID 4284—
反応物DiethylenetriamineHCID 8111—
反応物Phosphorus oxychlorideHCID 24813—
反応物2,5-Dimethyl-3-furoic acidHCID 69465—
反応物Methyl 4-chloroanthranilateHCID 80001—
反応物DiisopropylethylamineHCID 81531—
溶媒1,2-DichloroethaneHCID 11—
溶媒DimethylacetamideHCID 31374—
生成物4-Chloro-2-{[(2,5-dimethylfuran-3-yl)carbonyl]amino}benzoic acidHCID 16123491—

反応手順

In a 2 mL vial, methyl 2-amino-4-chlorobenzoate (7.4 mg, 40 μmol) was dissolved into a mixture of 655 μL DCE and 120 μL DMA, followed by addition of DIPEA (600 μmol, 15 eq.). 2,5-Dimethylfuran-3-carboxylic acid (16.8 mg, 120 μmol, 3 eq.) and POCl3 (18.2 mg, 120 μmol, 3 eq.) were added. The reaction mixture was capped and stirred at room temperature overnight. Another 700 μL of DCE was added to the reaction mixture along with the following resin bound reagents: a resin bound diethylene triamine (PL-DETA, Polymer Labs, 297 μmol, 7.4 eq.) and a hydroxide ion exchange resin (PL-MP Hydroxide, Polymer Labs, 800 μmol, 20 eq.). The vial was recapped and shaken at room temperature overnight. The resin in the reaction mixture was filtered off, rinsed with 300 μL of MeOH and discarded. The combined filtrates were concentrated down in vacuo. The residue was re-dissolved into 1 mL of DMA and 280 μL of 1M aqueous NaOH. The solution was stirred at room temperature overnight. The desired product was isolated directly from this solution via reverse phase C18 preparative HPLC (water/acetonitrile w/0.1% formic acid, 30%-100% eluant gradient) to yield the final product (2.3 mg, 95% purity). MS (EI) for C14H12ClNO4: 294 (M+H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08053454B2
出典データセットuspto-grants-2011_11
ORD IDord-5141b51707c242cf87f822a295917b73
出典メモuspto-grants-2011_11