Water → 2-(1-Amino-1-methylethyl)-4,5-bis(4-methoxyphenyl)thiazole hydrochloride

HRID 1885562ノート

反応式

HRID 1885562 の反応式
[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([C:9](=O)[CH:10]([C:12]2[CH:17]=[CH:16][C:15]([O:18][CH3:19])=[CH:14][CH:13]=2)[Cl:11])=[CH:5][CH:4]=1.C(OC([NH:28][C:29]([CH3:34])([CH3:33])[C:30](=[S:32])[NH2:31])=O)(C)(C)C.O>CN(C)C=O>[ClH:11].[NH2:28][C:29]([C:30]1[S:32][C:10]([C:12]2[CH:17]=[CH:16][C:15]([O:18][CH3:19])=[CH:14][CH:13]=2)=[C:9]([C:6]2[CH:7]=[CH:8][C:3]([O:2][CH3:1])=[CH:4][CH:5]=2)[N:31]=1)([CH3:34])[CH3:33]

参加物

5

反応物 3

HCID 962WaterHCID 38625232-Chloro-1,2-bis(4-methoxyphenyl)ethan-1-oneHCID 15186362tert-butyl N-(1-carbamothioyl-1-methylethyl)carbamate

生成物 1

HCID 197489022-(1-Amino-1-methylethyl)-4,5-bis(4-methoxyphenyl)thiazole hydrochloride収率 81.8%

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

反応条件

温度
70 °C

実験手順

A mixture of 1,2-bis(4-methoxyphenyl)-2-chloroethanone (5.00 g) and 2-tert-butyloxycarbonylamino-2-methylpropanethioamide (4.50 g) in dimethylformamide (25 ml) was stirred at 70° C. for 6 hours. After allowing to cool to the ambient temperature, the reaction mixture was dropped into water. The precipitates were collected by filtration. The resulting residue (6.28 g) was dissolved with dichloromethane (120 ml), and stirred at 2° C. To the reaction mixture was added 1,4-dioxan solution of 4N hydrogen chloride (60 ml), and stirred at ambient temperature for 1 hour. The resulting residue was evaporated in vacuo. The residue was added iso-propyl ether (300 ml) and stirred at 2° C. for 3 hours. The resulting precipitate was collected by filtration and washed with iso-propyl ether, to give 2-(1-amino-1-methylethyl)-4,5-bis(4-methoxyphenyl)thiazole hydrochloride (5.5 g).

後処理

  1. temperatureto cool to the ambient temperature
  2. filtrationThe precipitates were collected by filtration
  3. dissolutionThe resulting residue (6.28 g) was dissolved with dichloromethane (120 ml)
  4. stirringstirred at 2° C
  5. additionTo the reaction mixture was added 1,4-dioxan solution of 4N hydrogen chloride (60 ml)
  6. stirringstirred at ambient temperature for 1 hour
  7. customThe resulting residue was evaporated in vacuo
  8. additionThe residue was added iso-propyl ether (300 ml)
  9. stirringstirred at 2° C. for 3 hours
  10. filtrationThe resulting precipitate was collected by filtration
  11. washwashed with iso-propyl ether

出典と根拠

ORDレコード
ord-d62f0af2eacb44f9989db73b79f9ddd0
出典データセット
uspto-grants-1992_09
特許番号
US05145860

反応ノート

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