반응 #166326

반응 방정식

Compound 229

7-Cyclopentyl-2-(methylthio)-7H-pyrrolo[2,3-d]pyrimidine-6-carbaldehyde

N-chlorosuccinimide

water

bicarbonate

NCS

→

5-chloro-7-cyclopentyl-2-(methylthio)-7H-pyrrolo[2,3-d]pyrimidine-6-carbaldehyde

수율 39.0%

5-Chloro-7-cyclopentyl-2-(methylthio)-7H-pyrrolo[2,3-d]pyrimidine-6-carbaldehyde

수율 39.0%

용매

DMF

반응 조건

후처리

1. 1
   기타was reduced to 65° C.
2. 2
   workup.WAITAfter 30 min
3. 3
   기타the reaction contents
4. 4
   workup.ADDITIONwas added (300 mL)
5. 5
   추출The aqueous layer was extracted with dichloromethane (3×100 mL)
6. 6
   건조The combined organics were dried with sodium sulfate
7. 7
   농축concentrated in vacuo
8. 8
   세척Silica gel chromatography (gradient elution 0 to 7% ethyl acetate in hexanes)

실험 절차

Compound 229 (3.10 g, 11.9 mmol) and N-chlorosuccinimide (1.74 g, 13.0 mmol) were dissolved in DMF (30 mL) and stirred at 100° C. After 1 h, the temperature of the reaction was reduced to 65° C. and 0.35 eq of NCS were added. After 30 min, the reaction contents were poured into water (10×) and saturated bicarbonate was added (300 mL). The aqueous layer was extracted with dichloromethane (3×100 mL). The combined organics were dried with sodium sulfate and concentrated in vacuo. Silica gel chromatography (gradient elution 0 to 7% ethyl acetate in hexanes) afforded 5-chloro-7-cyclopentyl-2-(methylthio)-7H-pyrrolo[2,3-d]pyrimidine-6-carbaldehyde (230) (1.37 g, 39% yield). 1H NMR (500 MHz, CDCl3) δ ppm 10.17 (s, 1 H) 8.91 (s, 1 H) 5.73-5.96 (m, 1 H) 2.63 (s, 3 H) 2.29-2.47 (m, 2 H) 1.97-2.16 (m, 4 H) 1.63-1.83 (m, 2 H) ppm.

출처