반응 #90010
ord-f6bef84f4e634f30a2ee33747ce7b2c4
반응 방정식
반응물
시약
없음
용매
반응 조건
온도
120°CELSIUS
상세 조건
See reaction.notes.procedure_details.
후처리
- 1온도After cooling to room temperature
- 2기타purification
- 3기타to obtain the target compound (white powder, 12.8 mg, 34%)
실험 절차
Trifluoro-methanesulfonic acid 3-cyano-6,6-dimethyl-11-oxo-6,11-dihydro-5H-benzo[b]carbazol-8-yl ester (Compound B1, 40 mg, 0.0921 mmol) was dissolved in NMP (1 ml) and added with 1-isopropylpiperazine (236 mg, 20 eq.). The mixture was stirred at 120° C. for 3 hr. After cooling to room temperature, purification was carried out by HPLC to obtain the target compound (white powder, 12.8 mg, 34%).