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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 455481Erstellt: 24. Oktober 2026

4-Chloro-3-hydroxybenzoic acid → (4-Chloro-3-hydroxy-phenyl)-(cis-2,3,4,4a,9,9a-hexahydro-indeno[2,1-b]pyridin-1-yl)-methanone

https://huagongshe.com/de/reaction/455481

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-Chloro-3-hydroxybenzoic acidHCID 141872—
EduktMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
Eduktcis-2,3,4,4a,9,9a-hexahydro-1H-indeno[2,1-b]pyridineHCID 58123900—
Produkt(4-Chloro-3-hydroxy-phenyl)-(cis-2,3,4,4a,9,9a-hexahydro-indeno[2,1-b]pyridin-1-yl)-methanoneHCID 6796913344%

Reaktionsschritte

The title compound is prepared from 4-chloro-3-hydroxy-benzoic acid and cis-2,3,4,4a,9,9a-hexahydro-1H-indeno[2,1-b]pyridine following a procedure analogous to that described in Example 1 [2-(7-aza-1H-benzotriazol-1-yl)-1,1,3,3-tetramethyluronium hexafluorophosphate is used]. Yield: 44% of theory; LC (method 4): tR=1.97 min; Mass spectrum (ESI+): m/z=328 [M+H]+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08497281B2
Quelldatensatzuspto-grants-2013_07
ORD IDord-068b62aaa45543c081be6dff52a96348
Quellennotizuspto-grants-2013_07