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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 555928생성일: 2026년 10월 26일

Hydroxide → 2-[(1-Benzothien-3-ylcarbonyl)amino]-4-chlorobenzoic acid

https://huagongshe.com/reaction/555928

반응식

참여 물질

역할이름HCID투입량
반응물HydroxideHCID 961—
반응물N,N-diethyl-m-toluamideHCID 4284—
반응물DiethylenetriamineHCID 8111—
반응물Phosphorus oxychlorideHCID 24813—
반응물Methyl 4-chloroanthranilateHCID 80001—
반응물DiisopropylethylamineHCID 81531—
반응물Benzo(b)thiophene-3-carboxylic acidHCID 601280—
용매1,2-DichloroethaneHCID 11—
용매DimethylacetamideHCID 31374—
생성물2-[(1-Benzothien-3-ylcarbonyl)amino]-4-chlorobenzoic acidHCID 16123490—

반응 단계

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.). Benzo[b]thiophene-3-carboxylic acid (21.4 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 (2.9 mg, 95% purity). MS (EI) for C16H10ClNO3S: 332 (M+H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08053454B2
출처 데이터셋uspto-grants-2011_11
ORD IDord-4c60364aaf524e57b294bb048097d471
출처 메모uspto-grants-2011_11