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

HRID 463889
ノート
印刷プレビュー

反応式

HRID 463889 の反応式
[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]
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

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

生成物 1

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

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

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.

後処理

  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

出典と根拠

ORDレコード
ord-497c4e29233b4cd08a8198ebb07038bf
出典データセット
uspto-grants-1985_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04544752

反応ノート

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