반응 #11640
ord-76889c47bc604c94bffd53a4958f5462
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반응 조건
상세 조건
See reaction.notes.procedure_details.
후처리
- 1기타The named compound is prepared
- 2기타solvent evaporation in vacuo, trituration
- 3여과with isopropanol and filtration the reaction
실험 절차
The named compound is prepared by refluxing 0.020 gms E & Z 3-hydroxymethylene-6-(3-methoxy-phenyl)-1,3-dihydro-indol-2-one (see example 268) with 0.0375 gms 4-(3-piperidin-1-yl-propoxy)-phenylamine (used in the preparation of Example 218) in tetrahydrofuran (0.33 mL) for 36 h. Following cooling to room temperature, solvent evaporation in vacuo, trituration with isopropanol and filtration the reaction yields the named compound as a solid in the amount of 16.8 mg.