HRID1164844

反应详情

EQUATION

反应方程式

HRID 1164844 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

Combine the product of step A (12.2 g) with sodium azide (3.9 g) in DMF (200 ml). Stir 44 hours, extract with ethyl acetate, wash with water, dry the organic layer over MgSO4 and concentrate. Dissolve the resultant residue in ethanol (150 ml), add 5.0 g 10% Pd/C and hydrogenate at 3 atm for 4 hours. Filter and concentrate the filtrate to obtain 2-(2-aminoethyl)-6-chloro-3,4-dihydro-1,1-dioxo-7-sulfamoyl-1,2,4-benzothiadiazine. C. Treat the product of step B with N-(t-butoxycarbonyl)-(S)-aspartic acid, o-ethyl ester as described in Example 5, step A, and continue the procedure described in Example 5, steps B through F to obtain the title compound.

WORKUP

后处理

  1. extractionextract with ethyl acetate
  2. washwash with water
  3. dry with materialdry the organic layer over MgSO4
  4. concentrationconcentrate
  5. dissolutionDissolve the resultant residue in ethanol (150 ml)
  6. additionadd 5.0 g 10% Pd/C
  7. waithydrogenate at 3 atm for 4 hours
  8. filtrationFilter
  9. concentrationconcentrate the filtrate