HRID880239

反应详情

EQUATION

反应方程式

HRID 880239 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

4

PROCEDURE

实验过程

Dissolve 2-(3-methoxyphenyl)-4-(4-nitrophenyl)sulfonyl-morpholine (11.2 g, 29.6 mmol) in ACN (150 mL) and water (2.67 mL). Add LiOH (6.21 g, 147.99 mmol) while stirring the mixture and followed by 1-propanethiol (13.42 mL, 147.99 mmol). Stir the mixture for 25 h at ambient temperature. Dilute the mixture with EtOAc and add brine. Extract twice with EtOAc. Collect and concentrate the extracts to ˜200 mL under reduced pressure, then wash three times with 1N HCl. Combine the aqueous acid extracts and add Na2CO3 until the mixture is basic. Extract the basic solution three times with EtOAc; combine the extracts; wash the extracts with brine; and dry over Na2SO4. Filter; collect the filtrate; and remove the solvents under reduced pressure to provide a residue. Purify the residue via flash column chromatography eluting with EtOAc, followed by a 5-100% gradient of (10% 2M NH3 in MeOH)/DCM. Combine the product fractions, and remove the solvents under reduced pressure to provide the title compound as a yellow oil (3.09 g, 15.99 mmol). MS (m/z): 194 (M+1).

WORKUP

后处理

  1. extractionExtract twice with EtOAc
  2. customCollect
  3. concentrationconcentrate the extracts to ˜200 mL under reduced pressure
  4. washwash three times with 1N HCl
  5. additionadd Na2CO3 until the mixture
  6. extractionExtract the basic solution three times with EtOAc
  7. washwash the extracts with brine
  8. dry with materialand dry over Na2SO4
  9. filtrationFilter
  10. customcollect the filtrate
  11. customand remove the solvents under reduced pressure
  12. customto provide a residue
  13. customPurify the residue via flash column chromatography
  14. washeluting with EtOAc
  15. customremove the solvents under reduced pressure