3-ethoxycarbonylmethyl-6-fluoro-5-nitro-2(3H)-benzothiazolone → 5-amino-3-ethoxycarbonylmethyl-6-fluoro-2(3H)-benzothiazolone

HRID 477597Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 477597
[CH2:1]([O:3][C:4]([CH2:6][N:7]1[C:11]2[CH:12]=[C:13]([N+:17]([O-])=O)[C:14]([F:16])=[CH:15][C:10]=2[S:9][C:8]1=[O:20])=[O:5])[CH3:2]>C(O)(=O)C.C(OCC)(=O)C.[Fe]>[NH2:17][C:13]1[C:14]([F:16])=[CH:15][C:10]2[S:9][C:8](=[O:20])[N:7]([CH2:6][C:4]([O:3][CH2:1][CH3:2])=[O:5])[C:11]=2[CH:12]=1

Komponenten

5

Edukt 1

HCID 140142443-ethoxycarbonylmethyl-6-fluoro-5-nitro-2(3H)-benzothiazolone

Produkt 1

HCID 140142455-amino-3-ethoxycarbonylmethyl-6-fluoro-2(3H)-benzothiazoloneAusbeute 71,7 %

Reagenzien, Katalysatoren, Lösungsmittel 3

HCID 23925IronKatalysatorHCID 176Acetic AcidLösungsmittel2×HCID 8857Ethyl AcetateLösungsmittel

Versuchsvorschrift

Electrolytic iron powder (0.29 g) was suspended in 5% acetic acid (2 ml), and a solution of 3-ethoxycarbonylmethyl-6-fluoro-5-nitro-2(3H)-benzothiazolone (0.31 g) in acetic acid (1 ml) and ethyl acetate (1 ml) was dropwise added thereto while heating. The resultant mixture was heated under reflux for 3 hours. The reaction mixture was subjected to filtration with celite, and the filtrate was extracted with ethyl acetate. The extract was washed with water and sodium bicarbonate solution, dried and concentrated to give 0.20 g of 5-amino-3-ethoxycarbonylmethyl-6-fluoro-2(3H)-benzothiazolone. m.p., 172.5°-173.5° C.

Aufarbeitung

  1. temperaturewhile heating
  2. temperatureunder reflux for 3 hours
  3. filtrationThe reaction mixture was subjected to filtration with celite
  4. extractionthe filtrate was extracted with ethyl acetate
  5. washThe extract was washed with water and sodium bicarbonate solution
  6. customdried
  7. concentrationconcentrated

Quellen und Nachweise

ORD-Eintrag
ord-74511024267542968a8c318fedce1e25
Quelldatensatz
uspto-grants-1989_12
Patentnummer
US04888428

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