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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1761481Erstellt: 27. Oktober 2026

Ethanol → 1-acetyl-N-(2-benzothiazolyl)-4-piperidinemethanamine

https://huagongshe.com/reaction/1761481

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthanolHCID 702—
EduktCarbon TetrachlorideHCID 5943—
EduktBromineHCID 24408—
EduktN-[(1-acetyl-4-piperidinyl)methyl]-N'-phenylthioureaHCID 14048941—
LösungsmittelAcetonitrileHCID 6342—
Produkt1-acetyl-N-(2-benzothiazolyl)-4-piperidinemethanamineHCID 14048944—

Reaktionsschritte

To a stirred mixture of 5.8 parts of N-[(1-acetyl-4-piperidinyl)methyl]-N'-phenylthiourea and 160 parts of tetrachloromethane were added 3.7 parts of bromine. The whole was stirred and refluxed for 15 minutes. After the additions of 16 parts of ethanol and 16 parts of acetonitrile, the reaction mixture was cooled. The precipitated product was filtered off, washed with acetonitrile and dried. The hydrobromide salt was dissolved in methanol and water. This solution was alkalized with ammonium hydroxide. The precipitated product was filtered off, washed with water and dried, yielding 2.7 parts of 1-acetyl-N-(2-benzothiazolyl)-4-piperidinemethanamine; m.p. 138.1° C. (intermediate 29).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04826848
Quelldatensatzuspto-grants-1989_05
ORD IDord-195ab02ac0d84a80ad340df7b0963ed2
Quellennotizuspto-grants-1989_05