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Methylamine → N-methyl 3-(3-trifluoromethylphenyl)-4-amino-5-isothiazolecarboxamide

HRID 463889
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 463889
[CH3:1][NH2:2].[F:3][C:4]([F:23])([F:22])[C:5]1[CH:6]=[C:7]([C:11]2[C:15]([NH2:16])=[C:14]([C:17](OCC)=[O:18])[S:13][N:12]=2)[CH:8]=[CH:9][CH:10]=1>CO>[CH3:1][NH:2][C:17]([C:14]1[S:13][N:12]=[C:11]([C:7]2[CH:8]=[CH:9][CH:10]=[C:5]([C:4]([F:23])([F:22])[F:3])[CH:6]=2)[C:15]=1[NH2:16])=[O:18]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 2

HCID 6329MethylamineHCID 13532972Ethyl 3-(3-trifluoromethylphenyl)-4-amino-5-isothiazolecarboxylate

Produkt 1

HCID 13073259N-methyl 3-(3-trifluoromethylphenyl)-4-amino-5-isothiazolecarboxamide

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 887MethanolLösungsmittel

Versuchsvorschrift

One hundred ml. of methanol were saturated with gaseous methyl amine. Two grams of ethyl 3-(3-trifluoromethylphenyl)-4-amino-5-isothiazolecarboxylate were added. The reaction mixture was stirred at ambient temperature for about 30 minutes and was then heated to refluxing temperature for about 30 minutes. TLC indicated some amide had formed. Gaseous methylamine was bubbled through the refluxing reaction mixture for about 4 additional hours, at which time TLC indicated starting material was no longer present. The reaction mixture was poured into an ice-water mixture. N-methyl 3-(3-trifluoromethylphenyl)-4-amino-5-isothiazolecarboxamide formed in the above reaction precipitated and the precipitate collected by filtration. M.P. 113° C. (after vacuum drying). Yield 1.4 g.

Aufarbeitung

  1. temperaturewas then heated
  2. temperatureto refluxing temperature for about 30 minutes
  3. customhad formed
  4. customGaseous methylamine was bubbled through the refluxing reaction mixture for about 4 additional hours, at which time TLC
  5. additionThe reaction mixture was poured into an ice-water mixture

Quellen und Nachweise

ORD-Eintrag
ord-497c4e29233b4cd08a8198ebb07038bf
Quelldatensatz
uspto-grants-1985_10
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US04544752

Notizen zur Reaktion

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