反应 #167405

反应方程式

1-(benzothiazol-6-ylamino)-butan-2-one

Triethylamine

DPPA

nicotinic acid

→

product

收率 1.5%

1-Benzothiazol-6-yl-4-ethyl-3-pyridin-3-yl-1,3-dihydro-imidazol-2-one

收率 1.5%

溶剂

DCM

MeOH

toluene

反应条件

后处理

1. 1
   温度to reflux at 70° C. for 1.5 hours
2. 2
   其他The resulting reaction mass
3. 3
   温度was heated at 100° C. overnight
4. 4
   温度The reaction mixture was cooled to room temperature
5. 5
   浓缩concentrated under reduced pressure
6. 6
   其他the crude residue was partitioned between water and DCM
7. 7
   洗涤The organic layer was washed with water, brine solution
8. 8
   其他dried over Na2S4
9. 9
   浓缩concentrated
10. 10
    其他to afford the crude product
11. 11
    其他Purification by column chromatography on silica gel (1.5% methanol in chloroform)

实验过程

Triethylamine (0.2 mL, 1.219 mmol) and DPPA (0.3 mL, 1.219 mmol) were added to a solution of nicotinic acid (150 mg, 1.219 mmol) in toluene (12 mL) under nitrogen atmosphere and stirred at room temperature for 1.5 hours. The reaction mixture was allowed to reflux at 70° C. for 1.5 hours. The reaction was monitored by TLC (5% MeOH in DCM). This was followed by the addition of 1-(benzothiazol-6-ylamino)-butan-2-one (I-168a: 241 mg, 1.097 mmol) at room temperature. The resulting reaction mass was heated at 100° C. overnight. The reaction mixture was cooled to room temperature, concentrated under reduced pressure and the crude residue was partitioned between water and DCM. The organic layer was washed with water, brine solution, dried over Na2S4 and concentrated to afford the crude product. Purification by column chromatography on silica gel (1.5% methanol in chloroform) followed by preparative HPLC afforded 5 mg of the product (1.5% yield).

来源