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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2235076Erstellt: 26. Oktober 2026

Diisopropylethylamine → 2-chloro-4-[(1H-indole-6-carbonyl)-amino]-benzoic acid methyl ester

https://huagongshe.com/reaction/2235076

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiisopropylethylamineHCID 81531—
Edukt1H-indole-6-carboxylic acidHCID 595230—
EduktPyBroPHCID 2733179—
EduktMethyl 4-Amino-2-chlorobenzoateHCID 11839197—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt2-chloro-4-[(1H-indole-6-carbonyl)-amino]-benzoic acid methyl esterHCID 6869737426%

Reaktionsschritte

Bromo-tris-pyrrolidino-phosphonium hexafluorophosphate (8.3 g, 17.8 mmol, 1.1 equiv.) and diisopropyl ethyl amine (4.4 ml, 33.9 mmol, 2.1 equiv.) were added to 1H-indole-6-carboxylic acid (2.6 g, 16.2 mmol, 1 equiv.) in tetrahydrofuran (30 mL) and the mixture was shaken for 5 minutes at room temperature. 4-Amino-2-chlorobenzoic acid methyl ester (3.3 g, 17.9 mmol, 1.1 equiv.) was added and the resultant mixture was shaken at room temperature for 16 hours. The solvent was removed under vacuum and the residue triturated with dichloromethane (10 mL). The solid was filtered to afford 2-chloro-4-[(1H-indole-6-carbonyl)-amino]-benzoic acid methyl ester, 1.4 g (26% yield). LC @215 nm; Rt 1.36: 90%, m/z (ES+): 329 (M+H+.); δH (400 MHz; d6-DMSO) 11.65 (1H, s), 10.59 (1H, s), 8.16 (1H, s), 8.10 (1H, s), 7.93 (2H, m), 7.65 (2H, s), 7.59 (1H, m), 6.62 (1H, s), 3.85 (3H, s).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07713996B2
Quelldatensatzuspto-grants-2010_05
ORD IDord-f6120e17224a4b6085e2cad556988c9b
Quellennotizuspto-grants-2010_05