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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1014414Erstellt: 26. Oktober 2026

2-Amino-4-methylbenzamide → 2-({2-chloro-7-[(4-methylphenyl)sulfonyl]-7H-pyrrolo[2,3-d]pyrimidin-4-yl}amino)-4-methylbenzamide

https://huagongshe.com/reaction/1014414

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-Amino-4-methylbenzamideHCID 2801474—
Edukt2,4-dichloro-7-tosyl-7H-pyrrolo[2,3-d]pyrimidineHCID 53486828—
Produkt2-({2-chloro-7-[(4-methylphenyl)sulfonyl]-7H-pyrrolo[2,3-d]pyrimidin-4-yl}amino)-4-methylbenzamideHCID 86644183—

Reaktionsschritte

Using General Protocol II and starting with 2,4-dichloro-7-[(4-methylphenyl)sulfonyl]-7H-pyrrolo[2,3-d]pyrimidine (3.0 g, 8.8 mmol) and 2-amino-4-methylbenzamide (2.0 g, 13.2 mmol), 2-({2-chloro-7-[(4-methylphenyl)sulfonyl]-7H-pyrrolo[2,3-d]pyrimidin-4-yl}amino)-4-methylbenzamide was isolated as a white solid (2.81 g, 70% Yield): 1H NMR (400 MHz, DMSO-d6) δ ppm 2.34 (s, 3 H), 2.36 (s, 3 H), 6.65 (d, J=3.84 Hz, 1 H), 6.98 (s, 1 H), 7.47 (d, J=8.05 Hz, 2 H), 7.70 (s, 1 H), 7.74 (s, 1 H), 7.75 (d, J=2.93 Hz, 1 H), 7.98 (d, J=8.42 Hz, 2 H), 8.25 (s, 1 H), 8.33 (s, 1 H), 12.52 (s, 1 H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07981903B2
Quelldatensatzuspto-grants-2011_07
ORD IDord-7c43697587b84e69a76171809b2358ce
Quellennotizuspto-grants-2011_07