Hydrochloric Acid → HCID 69698838、化合物
反応式
C([NH:5][C:6]([NH:8][C@@H:9]([CH2:13][C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1)[CH:10](O)[CH3:11])=[S:7])(C)(C)C.Cl>O>[CH2:13]([C@H:9]1[C@H:10]([CH3:11])[S:7][C:6]([NH2:5])=[N:8]1)[C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1参加物
反応条件
- 温度
- 100 °C
実験手順
The process is performed as in Example 3, starting with 3.9 g of diastereoisomer A of the N-(tert-butyl)-N′-((1S)-1-benzyl-2-hydroxypropyl)thiourea in 46 cm3 of aqueous 6N hydrochloric acid. After heating for 5 hours at a temperature in the region of 100° C., the reaction mass is concentrated under reduced pressure (5 kPa) at a temperature in the region of 50° C. The oil obtained is dissolved in 50 cm3 of water; the solution is washed with twice 50 cm3 of dichloromethane. The aqueous phase is made alkaline by addition of 3 cm3 of 30% caustic soda and then extracted with 3 times 50 cm3 of dichloromethane. The organic extracts are combined and dried over sodium sulfate. After filtration and concentration under reduced pressure (5 kPa) at a temperature in the region of 40° C., 2.5 g of (−)-(4S,5S)-4-benzyl-5-methyl-4,5-dihydro-1,3-thiazol-2-ylamine are obtained in the form of a white solid melting at 89° C. (trans isomer). (αD20=−87.3±1.3 at a concentration of 0.5% in methanol).
後処理
- concentrationthe reaction mass is concentrated under reduced pressure (5 kPa) at a temperature in the region of 50° C
- customThe oil obtained
- washthe solution is washed with twice 50 cm3 of dichloromethane
- additionby addition of 3 cm3 of 30% caustic soda
- extractionextracted with 3 times 50 cm3 of dichloromethane
- dry with materialdried over sodium sulfate
- filtrationAfter filtration and concentration under reduced pressure (5 kPa) at a temperature in the region of 40° C., 2.5 g of (−)-(4S,5S)-4-benzyl-5-methyl-4,5-dihydro-1,3-thiazol-2-ylamine
出典と根拠
- ORDレコード
- ord-8207a29a2ca34bfbb06ac18884f45932
- 出典データセット
- uspto-grants-2004_03
- 特許番号
- US06699895B2
反応ノート
読み込み中…