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

HRID 463889
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HRID 463889 반응식
[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]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

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

생성물 1

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

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

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.

후처리

  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

출처 및 근거

ORD 기록
ord-497c4e29233b4cd08a8198ebb07038bf
출처 데이터셋
uspto-grants-1985_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04544752

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