Hydrochloric Acid → 4-[2-(4-Chlorophenyl)-6-(hexahydropyrrolo[3,4-c]pyrrol-2-yl)imidazo[1,2-b]pyridazin-3-yl]pyrid-2-ylamine
반응식
[NH2:1][C:2]1[CH:7]=[C:6]([C:8]2[N:12]3[N:13]=[C:14]([N:17]4[CH2:21][CH:20]5[CH2:22][N:23](C(OCCCC)=O)[CH2:24][CH:19]5[CH2:18]4)[CH:15]=[CH:16][C:11]3=[N:10][C:9]=2[C:32]2[CH:37]=[CH:36][C:35]([Cl:38])=[CH:34][CH:33]=2)[CH:5]=[CH:4][N:3]=1.Cl>ClCCl>[Cl:38][C:35]1[CH:36]=[CH:37][C:32]([C:9]2[N:10]=[C:11]3[CH:16]=[CH:15][C:14]([N:17]4[CH2:21][CH:20]5[CH:19]([CH2:24][NH:23][CH2:22]5)[CH2:18]4)=[N:13][N:12]3[C:8]=2[C:6]2[CH:5]=[CH:4][N:3]=[C:2]([NH2:1])[CH:7]=2)=[CH:33][CH:34]=1참가 물질
4
반응물 2
생성물 1
시약·촉매·용매 1
실험 절차
To a solution of 0.16 g (0.29 mmol) of tent-butyl 5-[3-(2-aminopyrid-4-yl)-2-(4-chlorophenyl)-imidazo[1,2-b]pyridazin-6-yl]hexahydropyrrolo[3,4-c]pyrrole-2-carboxylate in 3 mL of dichloromethane are added 1.5 mL (18 mmol) of concentrated hydrochloric acid. After stirring for 1 hour at room temperature, the solvent is evaporated off under reduced pressure, the oily residue is taken up with aqueous ammonia and the product is extracted with dichloromethane. The organic phase is filtered on a hydrophobic cartridge and concentrated under reduced pressure. The solid obtained is triturated with diisopropyl ether to give 0.091 g of solid after filtering off and drying under reduced pressure.
후처리
- customthe solvent is evaporated off under reduced pressure
- extractionthe product is extracted with dichloromethane
- filtrationThe organic phase is filtered on a hydrophobic cartridge
- concentrationconcentrated under reduced pressure
- customThe solid obtained
- customis triturated with diisopropyl ether
출처 및 근거
- ORD 기록
- ord-5c97f2eab17c4b80ac937622befab148
- 출처 데이터셋
- uspto-grants-2013_01
- 특허 번호
- US08354405B2
반응 노트
불러오는 중…