Diisopropylethylamine → HCID 131737175, 화합물

HRID 61425노트

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HRID 61425 반응식
[C:1]([O:5][C:6]([CH:8]1[CH2:13][CH2:12][CH2:11][NH:10][CH:9]1C(O)=O)=[O:7])([CH3:4])([CH3:3])[CH3:2].[CH:17]([C:20]1[CH:21]=[C:22]([C:26]2[CH2:27][CH2:28]NCC=2)[CH:23]=[CH:24][CH:25]=1)([CH3:19])[CH3:18].C1CN([P+]([O:48]N2N=NC3C=CC=CC2=3)(N2CCCC2)N2CCCC2)CC1.F[P-](F)(F)(F)(F)F.[CH:65]([N:68]([CH:71](C)C)CC)(C)[CH3:66]>CN(C=O)C.CCOC(C)=O>[C:1]([O:5][C:6]([CH:8]1[CH:13]([C:71]([N:68]2[CH2:65][CH:66]=[CH:28][CH2:27][CH:26]2[C:22]2[CH:23]=[CH:24][CH:25]=[C:20]([CH:17]([CH3:18])[CH3:19])[CH:21]=2)=[O:48])[CH2:12][CH2:11][NH:10][CH2:9]1)=[O:7])([CH3:2])([CH3:3])[CH3:4]

참가 물질

7

실험 절차

To a 0° C. solution of piperidine-2,3-dicarboxylic acid 3-tert-butyl ester (100 mg) in DMF (0.6 mL) was added sequentially, 4-(3-isopropyl-phenyl)-1,2,3,6-tetrahydropyridine (97 mg). PyBOP (232 mg), and diisopropylethylamine (0.152 mL). The resultant mixture was stirred at rt overnight. The reaction solution was diluted with EtOAc and washed with saturated NaHCO3 solution (×3), water, and brine. The organic layers were dried over MgSO4, filtered, and concentrated to dry under reduced pressure. The residue was used in next step without further purifications. MS (ESI): 413.2 (M+H+)

후처리

  1. washwashed with saturated NaHCO3 solution (×3), water, and brine
  2. dry with materialThe organic layers were dried over MgSO4
  3. filtrationfiltered
  4. concentrationconcentrated
  5. customto dry under reduced pressure

출처 및 근거

ORD 기록
ord-b9786a318b304490bf004bef6f1818a3
출처 데이터셋
uspto-grants-2016_09
특허 번호
US09440958B2

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