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
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Diisopropylethylamine | HCID 81531 | — |
| Edukt | 1H-indole-6-carboxylic acid | HCID 595230 | — |
| Edukt | PyBroP | HCID 2733179 | — |
| Edukt | Methyl 4-Amino-2-chlorobenzoate | HCID 11839197 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | 2-chloro-4-[(1H-indole-6-carbonyl)-amino]-benzoic acid methyl ester | HCID 68697374 | 26% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07713996B2 |
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| Quelldatensatz | uspto-grants-2010_05 |
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| ORD ID | ord-f6120e17224a4b6085e2cad556988c9b |
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| Quellennotiz | uspto-grants-2010_05 |
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