반응 #619087

ord-588c028883fb47d381ff96a431d3dd91

반응 방정식

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

용매

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    workup.ADDITIONwas added
  2. 2
    건조The organic phase was dried (MgSO4)
  3. 3
    기타the solvent was removed in vacuo
  4. 4
    workup.ADDITIONMeCN (1 mL) was added whereupon the product
  5. 5
    기타precipitated
  6. 6
    여과The product was filtered off
  7. 7
    기타dried

실험 절차

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.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: USRE045183E1uspto-grants-2014_10