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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2235119Erstellt: 25. Oktober 2026

Benzocaine → HCID 68696720, Verbindung

https://huagongshe.com/reaction/2235119

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzocaineHCID 2337—
EduktMethyl indole-6-carboxylateHCID 639844—
EduktHCID 16051865HCID 16051865—
EduktMethyl 2,3-dihydro-1H-indole-6-carboxylateHCID 16244446—
Edukt1H-INDOLE-1,6-DICARBOXYLIC ACID,2,3-DIHYDRO-,1-(1,1-DIMETHYLETHYL)ESTERHCID 18354849—
Edukt1-tert-butyl 6-methyl 2,3-dihydro-1H-indole-1,6-dicarboxylateHCID 66575048—
ProduktHCID 68696720HCID 68696720—

Reaktionsschritte

4-{[1-(3,5-Dichloro-benzenesulfonyl)-2,3-dihydro-1H-indole-6-carbonyl]-amino}-benzoic acid, MS (ISP): m/e=488.9 (M−H), was prepared in analogy to example 14, steps 1 to 6. Step 1 was performed starting from 1H-indole-6-carboxylic acid methyl ester, which was reduced to 2,3-dihydro-1H-indole-6-carboxylic acid methyl ester (see also example 34). This was protected in step 2 to 2,3-dihydro-indole-1,6-dicarboxylic acid 1-tert-butyl ester 6-methyl ester, which was then hydrolyzed to 2,3-dihydro-indole-1,6-dicarboxylic acid 1-tert-butyl ester in step 3. Step 4 was performed using 4-amino-benzoic acid ethyl ester, yielding 4-[(2,3-dihydro-1H-indole-6-carbonyl)-amino]-benzoic acid ethyl ester. This was reacted with 3,5-dichloro-benzenesulfonyl chloride in step 5, yielding 4-{[1-(3,5-dichloro-benzenesulfonyl)-2,3-dihydro-1H-indole-6-carbonyl]-amino}-benzoic acid, which was hydrolyzed in step 6.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07713996B2
Quelldatensatzuspto-grants-2010_05
ORD IDord-996da454903e4198938d665a92b005cb
Quellennotizuspto-grants-2010_05