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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1427825Erstellt: 26. Oktober 2026

Tricyclo(3.3.1.1'3,7)dec-1-ylmethanol → 5-chloro-N-(N,N-dimethylsulfamoyl)-2-fluoro-4-(spiro[3.5]nonan-7-ylmethoxy)-benzamide

https://huagongshe.com/reaction/1427825

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTricyclo(3.3.1.1'3,7)dec-1-ylmethanolHCID 64556—
EduktSpiro[3.5]nonan-7-ylmethanolHCID 53487452—
Edukt5-chloro-2,4-difluoro-N-(methylsulfonyl)benzamideHCID 58042417—
Edukt5-chloro-N-(N,N-dimethylsulfamoyl)-2,4-difluorobenzamideHCID 86702836—
Produkt5-chloro-N-(N,N-dimethylsulfamoyl)-2-fluoro-4-(spiro[3.5]nonan-7-ylmethoxy)-benzamideHCID 86702851—

Reaktionsschritte

Following the procedure as described in Example 8 and making variations as required to replace 5-chloro-2,4-difluoro-N-(methylsulfonyl)benzamide with 5-chloro-N-(N,N-dimethylsulfamoyl)-2,4-difluorobenzamide and adamantan-1-ylmethanol with spiro[3.5]nonan-7-ylmethanol, the title compound was obtained as a colorless solid (0.26 g, 47%): 1H NMR (300 MHz, CDCl3) δ 8.61 (br s, 1H), 8.05 (d, J=8.4 Hz, 1H), 6.65 (d, J=13.5 Hz, 1H), 3.82 (d, J=6.3 Hz, 2H), 3.01 (s, 6H), 1.89-1.65 (m, 11H), 1.35-1.04 (m, 4H); MS (ES−) m/z: 431.2, 433.2 (M−1).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08933236B2
Quelldatensatzuspto-grants-2015_01
ORD IDord-430d4fd7dba84416b8a13a7d640a5667
Quellennotizuspto-grants-2015_01