Sodium borohydride → (2R,3R)-3-hydroxy-8-methyl-2-(4-methylphenyl)-2,3-dihydro-1,5-benzothiazepin-4(5H)-one

HRID 1033480

反応式

HRID 1033480 の反応式
N[C@@H](C(O)=O)C(C)(C)C.[BH4-].[Na+].[CH3:12][C:13]1[CH:32]=[CH:31][C:16]2[NH:17][C:18](=[O:30])[C:19](=[O:29])[CH:20]([C:22]3[CH:27]=[CH:26][C:25]([CH3:28])=[CH:24][CH:23]=3)[S:21][C:15]=2[CH:14]=1.C(O)(=O)C.O1CCCC1>O1CCCC1>[OH:29][C@@H:19]1[C:18](=[O:30])[NH:17][C:16]2[CH:31]=[CH:32][C:13]([CH3:12])=[CH:14][C:15]=2[S:21][C@@H:20]1[C:22]1[CH:23]=[CH:24][C:25]([CH3:28])=[CH:26][CH:27]=1

参加物

6

反応物 4

HCID 4311764Sodium borohydrideHCID 6950340D-tert-leucineHCID 190261378-methyl-2-(4-methyl-phenyl)-1,5-benzothiazepine-3,4(2H,5H)-dioneHCID 23444217Acetic acid tetrahydrofuran

生成物 1

HCID 10566075(2R,3R)-3-hydroxy-8-methyl-2-(4-methylphenyl)-2,3-dihydro-1,5-benzothiazepin-4(5H)-one収率 80.6%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒2 回

反応条件

温度
-15 °C

実験手順

A mixture of D-tert-leucine (721 mg), sodium borohydride (189 mg) and tetrahydrofuran (50 ml) is refluxed under nitrogen atmosphere for three hours. The mixture is cooled to -15° C., and thereto is added a solution of 8-methyl-2-(4-methylphenyl)-1,5-benzothiazepine-3,4(2H, 5H)-dione (991 mg) in tetrahydrofuran (3 ml). Each 0.38 ml of 25% acetic acid/tetrahydrofuran solution (1.67 mmole as acetic acid) is added thereto at 25 minutes, and 2 hours 10 minutes after the beginning of the reaction, and the reaction solution is stirred at the same temperature for 20 hours. The mixture is evaporated under reduced pressure to remove the solvent, and to the residue is added 1N hydrochloric acid (70 ml). The precipitated crystal is collected by filtration, washed with water, and dried. The collected crystal is suspended in isopropyl alcohol (12 ml), and the mixture is heated with stirring at 80° C. for three hours. The mixture is cooled to 5° C., and allowed to stand for five hours. The precipitated crystal is collected by filtration, washed with cold isopropyl alcohol, and dried to give (2R,3R)-3-hydroxy-8-methyl-2-(4-methylphenyl)-2,3-dihydro-1,5-benzothiazepin-4(5H)-one (804 mg).

後処理

  1. temperatureis refluxed under nitrogen atmosphere for three hours
  2. custom2 hours 10 minutes after the beginning of the reaction
  3. customThe mixture is evaporated under reduced pressure
  4. customto remove the solvent
  5. additionto the residue is added 1N hydrochloric acid (70 ml)
  6. filtrationThe precipitated crystal is collected by filtration
  7. washwashed with water
  8. customdried
  9. temperaturethe mixture is heated
  10. stirringwith stirring at 80° C. for three hours
  11. temperatureThe mixture is cooled to 5° C.
  12. waitto stand for five hours
  13. filtrationThe precipitated crystal is collected by filtration
  14. washwashed with cold isopropyl alcohol
  15. customdried

出典と根拠

ORDレコード
ord-9275edf4827441378485aeff29604116
出典データセット
uspto-grants-1994_05
特許番号
US05310904

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