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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1018303Erstellt: 26. Oktober 2026

N-Methyl-D-glucamine → 3-[(2-Adamantan-1-ylmethyl-5-phenyl-1h-pyrrole-3-carbonyl)-amino]-benzoic acid

https://huagongshe.com/reaction/1018303

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktN-Methyl-D-glucamineHCID 8567—
Edukt2-Adamantan-1-ylmethyl-5-phenyl-1h-pyrrole-3-carboxylic acidHCID 11382084—
EduktBenzyl 3-aminobenzoateHCID 15428374—
Edukt1,4-Dioxane--water (1/1)HCID 21886435—
LösungsmittelWaterHCID 962—
Produkt3-[(2-Adamantan-1-ylmethyl-5-phenyl-1h-pyrrole-3-carbonyl)-amino]-benzoic acidHCID 9890198—

Reaktionsschritte

The benzyl ester of the title compound was prepared by reacting 2-adamantan-1-ylmethyl-5-phenyl-1H-pyrrole-3-carboxylic acid (Example 1, step c) with 3-amino-benzoic acid benzyl ester according to the procedure of Example 1, step d. This was converted to the title compound using the procedure of Example 1, step e. 1H NMR (300 MHz, d6-DMSO) 11.19 (1H, s), 9.62 (1H, s), 8.37 (1H, s), 7.97 (1H, d) 7.66 (2H, d), 7.58 (1H, d), 7.39 (3H, m), 7.16 (2H, m), 2.84 (2H, s), 1.88 (3H, br s), 1.54 (12H, m). The product was converted to the N-methyl-D-glucamine salt and lyophilised from water/dioxan. Found: C, 62.82; H, 7.38; N, 5.82%; C36H47N3O8.2.0 H2O requires: C, 63.04; H, 7.50; N, 6.12%.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06479531B1
Quelldatensatzuspto-grants-2002_11
ORD IDord-02b53532c81e4d589a5a3aecb5cfe9e8
Quellennotizuspto-grants-2002_11