Diisopropylethylamine → [4-(3,4-Dichloro-phenoxy)-[1,4']bipiperidinyl-1'-yl]-(3-methanesulfonyl-phenyl)-methanone acetate

HRID 1060804노트

반응식

HRID 1060804 반응식
[Cl:1][C:2]1[CH:3]=[C:4]([CH:18]=[CH:19][C:20]=1[Cl:21])[O:5][CH:6]1[CH2:11][CH2:10][N:9]([CH:12]2[CH2:17][CH2:16][NH:15][CH2:14][CH2:13]2)[CH2:8][CH2:7]1.F[P-](F)(F)(F)(F)F.Br[P+](N1CCCC1)(N1CCCC1)N1CCCC1.[CH3:46][S:47]([C:50]1[CH:51]=[C:52]([CH:56]=[CH:57][CH:58]=1)[C:53]([OH:55])=[O:54])(=[O:49])=[O:48].C(N(CC)C(C)C)(C)C.C([O-])(O)=O.[Na+]>C1COCC1.C(OCC)(=O)C>[C:53]([OH:55])(=[O:54])[CH3:52].[Cl:1][C:2]1[CH:3]=[C:4]([CH:18]=[CH:19][C:20]=1[Cl:21])[O:5][CH:6]1[CH2:7][CH2:8][N:9]([CH:12]2[CH2:13][CH2:14][N:15]([C:53]([C:52]3[CH:56]=[CH:57][CH:58]=[C:50]([S:47]([CH3:46])(=[O:49])=[O:48])[CH:51]=3)=[O:54])[CH2:16][CH2:17]2)[CH2:10][CH2:11]1

참가 물질

8

실험 절차

The product of Step b (0.15 g) was dissolved in THF (4 ml), bromo-tris-pyrrolidino-phosphonium hexafluorophosphate (PYBROP™; 0.235 g), 3-methylsulphonylbenzoic acid (0.091 g) and N,N-di-iso-propylethylamine (0.238 ml) were added. After 18 hours at room temperature ethyl acetate and aqueous NaHCO3 solution were added. The product was extracted with ethyl acetate, the combined organic extracts dried with Na2SO4 and concentrated. Purification by reverse phase HPLC (with a gradient eluent system (45% MeCN/NH4OAcaq (0.1%) to 95% MeCN//NH4OAcaq (0.1%)) gave the title compound (0.095 g).

후처리

  1. extractionThe product was extracted with ethyl acetate
  2. dry with materialthe combined organic extracts dried with Na2SO4
  3. concentrationconcentrated
  4. customPurification by reverse phase HPLC (with a gradient eluent system (45% MeCN/NH4OAcaq (0.1%) to 95% MeCN//NH4OAcaq (0.1%))

출처 및 근거

ORD 기록
ord-5444b2f23f074b858538786132a5c9ff
출처 데이터셋
uspto-grants-2003_02
특허 번호
US06525070B2

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