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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 555928Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/555928

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydroxideHCID 961—
EduktN,N-diethyl-m-toluamideHCID 4284—
EduktDiethylenetriamineHCID 8111—
EduktPhosphorus oxychlorideHCID 24813—
EduktMethyl 4-chloroanthranilateHCID 80001—
EduktDiisopropylethylamineHCID 81531—
EduktBenzo(b)thiophene-3-carboxylic acidHCID 601280—
Lösungsmittel1,2-DichloroethaneHCID 11—
LösungsmittelDimethylacetamideHCID 31374—
Produkt2-[(1-Benzothien-3-ylcarbonyl)amino]-4-chlorobenzoic acidHCID 16123490—

Reaktionsschritte

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).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08053454B2
Quelldatensatzuspto-grants-2011_11
ORD IDord-4c60364aaf524e57b294bb048097d471
Quellennotizuspto-grants-2011_11