反应 #619108

ord-869e1bfa0afb4e099e2531c5bec5017b

反应方程式

O=C(Nc1nc(CO)cs1)N(C1CCCCC1)C1CCCCC1
1,1-dicyclohexyl-3-(4-hydroxymethyl-thiazol-2-yl)urea
O=S(=O)=O.c1ccncc1
pyridine-sulfur trioxide
CCN(CC)CC
triethyl-amine
O=Cc1csc(NC(=O)N(C2CCCCC2)C2CCCCC2)n1
1,1-dicyclohexyl-3-(4-formyl-thiazol-2-yl)urea
收率 95.2%

溶剂

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    其他quenched with water (50 mL)
  2. 2
    其他the layers were separated
  3. 3
    萃取The aqueous layer was extracted with DCM (2×50 mL)
  4. 4
    洗涤The combined organic layers was washed with water, saturated ammonium chloride solution, brine
  5. 5
    干燥dried over sodium sulfate
  6. 6
    浓缩concentrated in vacuo

实验过程

To a solution of 1,1-dicyclohexyl-3-(4-hydroxymethyl-thiazol-2-yl)urea (850 mg, 2.5 mmol) in 4:1 DCM/DMSO (8 mL) was added pyridine-sulfur trioxide (1.59 g, 10.0 mmol) and triethyl-amine (1.55 mL, 11.25 mmol) at 0° C. The mixture was stirred for 6 h and quenched with water (50 mL) and the layers were separated. The aqueous layer was extracted with DCM (2×50 mL). The combined organic layers was washed with water, saturated ammonium chloride solution, brine, dried over sodium sulfate and concentrated in vacuo to obtain 1,1-dicyclohexyl-3-(4-formyl-thiazol-2-yl)urea (800 mg, 2.38 mmol).

来源

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