反応 #619087

ord-588c028883fb47d381ff96a431d3dd91

反応方程式

O
water
O=C(Nc1nccs1)N(C1CCCCC1)N1CCCCC1
1-Cyclohexyl-1-piperidin-1-yl-3-thiazol-2-yl-urea
O=C1CCC(=O)N1Cl
NCS
O=C(Nc1ncc(Cl)s1)N(C1CCCCC1)N1CCCCC1
3-(5-Chloro-thiazol-2-yl)-1-cyclohexyl-1-piperidin-1-yl-urea

溶媒

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    workup.ADDITIONwas added
  2. 2
    乾燥The organic phase was dried (MgSO4)
  3. 3
    その他the solvent was removed in vacuo
  4. 4
    workup.ADDITIONMeCN (1 mL) was added whereupon the product
  5. 5
    その他precipitated
  6. 6
    ろ過The product was filtered off
  7. 7
    その他dried

実験手順

1-Cyclohexyl-1-piperidin-1-yl-3-thiazol-2-yl-urea (50 mg, 0.16 mmol), prepared in an identical manner to Example 94 was dissolved in DCM (1 mL) and NCS (26 mg, 0.19 mmol)) was added. The reaction mixture was stirred for 3 days before DCM (20 mL) and water (20 mL) was added. The organic phase was dried (MgSO4) and the solvent was removed in vacuo. MeCN (1 mL) was added whereupon the product precipitated. The product was filtered off and dried. Yield: 20 mg.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: USRE045183E1uspto-grants-2014_10