Triethylamine → 3-[[2-(1-tert-Butoxycarbonylpiperid-4-yl)ethyl]-amino]-5,6-dichloro-3-(2-chlorophenyl)-1,3-dihydroindol-2-one
반응식
[NH2:1][CH2:2][CH2:3][CH:4]1[CH2:9][CH2:8][N:7]([C:10]([O:12][C:13]([CH3:16])([CH3:15])[CH3:14])=[O:11])[CH2:6][CH2:5]1.C(N(CC)CC)C.Br[C:25]1([C:37]2[CH:42]=[CH:41][CH:40]=[CH:39][C:38]=2[Cl:43])[C:33]2[C:28](=[CH:29][C:30]([Cl:35])=[C:31]([Cl:34])[CH:32]=2)[NH:27][C:26]1=[O:36]>C(Cl)(Cl)Cl.C1COCC1>[C:13]([O:12][C:10]([N:7]1[CH2:6][CH2:5][CH:4]([CH2:3][CH2:2][NH:1][C:25]2([C:37]3[CH:42]=[CH:41][CH:40]=[CH:39][C:38]=3[Cl:43])[C:33]3[C:28](=[CH:29][C:30]([Cl:35])=[C:31]([Cl:34])[CH:32]=3)[NH:27][C:26]2=[O:36])[CH2:9][CH2:8]1)=[O:11])([CH3:16])([CH3:15])[CH3:14]참가 물질
6
반응물 3
생성물 1
시약·촉매·용매 2
실험 절차
A solution of 1.05 g of 4-(2-aminoethyl)-1-(tert-butoxycarbonyl)piperidine and 0.46 g of triethylamine in 10 ml of chloroform is added at RT to a solution of 1.8 g of the compound obtained in step C in 50 ml of THF and the mixture is stirred for 2 hours at RT. It is concentrated under vacuum, the residue is taken up with a 5% solution of potassium carbonate and extracted with AcOEt, the organic phase is washed with water and with a saturated solution of NaCl, boiling THF is added to the organic phase, the latter is dried over sodium sulfate and the solvents are partially evaporated off. The crystalline product formed is filtered off to give 1.94 g of the expected product.
후처리
- concentrationIt is concentrated under vacuum
- extractionextracted with AcOEt
- washthe organic phase is washed with water and with a saturated solution of NaCl
- additionis added to the organic phase
- dry with materialthe latter is dried over sodium sulfate
- customthe solvents are partially evaporated off
- customThe crystalline product formed
- filtrationis filtered off
출처 및 근거
- ORD 기록
- ord-c864e079998c4c23986f5857658cce08
- 출처 데이터셋
- uspto-grants-1997_01
- 특허 번호
- US05594023
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