Trifluoroacetic acid → 1-(2-(2-(2-(4-(1-Aminoethyl)phenylamino)-5-(trifluoromethyl)pyrimidin-4-yl)ethyl)phenyl)cyclopropanecarboxamide
반응식
[C:1]([C:4]1([C:7]2[CH:41]=[CH:40][CH:39]=[CH:38][C:8]=2[CH2:9][CH2:10][C:11]2[C:16]([C:17]([F:20])([F:19])[F:18])=[CH:15][N:14]=[C:13]([NH:21][C:22]3[CH:27]=[CH:26][C:25]([CH:28]([NH:30]C(=O)OC(C)(C)C)[CH3:29])=[CH:24][CH:23]=3)[N:12]=2)[CH2:6][CH2:5]1)(=[O:3])[NH2:2].FC(F)(F)C(O)=O>C(Cl)Cl>[NH2:30][CH:28]([C:25]1[CH:24]=[CH:23][C:22]([NH:21][C:13]2[N:12]=[C:11]([CH2:10][CH2:9][C:8]3[CH:38]=[CH:39][CH:40]=[CH:41][C:7]=3[C:4]3([C:1]([NH2:2])=[O:3])[CH2:5][CH2:6]3)[C:16]([C:17]([F:19])([F:20])[F:18])=[CH:15][N:14]=2)=[CH:27][CH:26]=1)[CH3:29]참가 물질
4
반응물 2
생성물 1
시약·촉매·용매 1
실험 절차
To a solution of tert-butyl 1-(4-(4-(2-(1-carbamoylcyclopropyl)phenethyl)-5-(trifluoromethyl)pyrimidin-2-ylamino)phenyl)ethylcarbamate 70 (0.11 g, 0.19 mmol) in DCM (4 mL) was added trifluoroacetic acid (2 mL). The mixture was stirred at ambient temperature for 16 hours before the volatiles were removed in vacuo. The crude residue was purified using an SCX conditioned with MeOH, product was eluted off with 2 M ammonia in EtOH) to give the title compound 70A as a cream solid (0.073 g, 81%). LCMS-C: rt 4.48 min; m/z 470 [M+H]+.
후처리
- customwere removed in vacuo
- customThe crude residue was purified
- washwas eluted off with 2 M ammonia in EtOH)
출처 및 근거
- ORD 기록
- ord-4fe429c53cb64e7182bc121bce42c63e
- 출처 데이터셋
- uspto-grants-2016_01
- 특허 번호
- US09238644B2
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