Hydrochloric Acid → N-[4-[(3S,5R)-3-amino-5-methylpiperidin-1-yl]-7-hydroxy-6,7-dihydro-5H-cyclopenta[b]pyridin-3-yl]-6-[2,6-difluoro-4-(oxan-3-yloxy)phenyl]-5-fluoropyridine-2-carboxamide

HRID 1499618노트

반응식

HRID 1499618 반응식
[F:1][C:2]1[CH:7]=[C:6]([O:8][CH:9]2[CH2:14][CH2:13][CH2:12][O:11][CH2:10]2)[CH:5]=[C:4]([F:15])[C:3]=1[C:16]1[N:21]=[C:20]([C:22]([NH:24][C:25]2[C:26]([N:35]3[CH2:40][C@H:39]([CH3:41])[CH2:38][C@H:37]([NH:42]C(=O)OC(C)(C)C)[CH2:36]3)=[C:27]3[CH2:33][CH2:32][CH:31]([OH:34])[C:28]3=[N:29][CH:30]=2)=[O:23])[CH:19]=[CH:18][C:17]=1[F:50].Cl.O1CCOCC1>>[NH2:42][C@H:37]1[CH2:38][C@@H:39]([CH3:41])[CH2:40][N:35]([C:26]2[C:25]([NH:24][C:22]([C:20]3[CH:19]=[CH:18][C:17]([F:50])=[C:16]([C:3]4[C:2]([F:1])=[CH:7][C:6]([O:8][CH:9]5[CH2:14][CH2:13][CH2:12][O:11][CH2:10]5)=[CH:5][C:4]=4[F:15])[N:21]=3)=[O:23])=[CH:30][N:29]=[C:28]3[CH:31]([OH:34])[CH2:32][CH2:33][C:27]=23)[CH2:36]1

참가 물질

4

실험 절차

The alcohol intermediate made above was treated with 4.0 M HCl in dioxane (1 mL, 5 mmol) at room temperature overnight. The solution was concentrated under reduced pressure and the resulting residue was purified by preparative LCMS (Waters SunFire™ C18 column, 19 mm×100 mm, 5 μm particle size, eluting with a gradient of MeCN/water containing 0.1% NH4OH, at flow rate of 30 mL/min.) to give two separated diastereoisomers of the title compound as white powders.

후처리

  1. concentrationThe solution was concentrated under reduced pressure
  2. customthe resulting residue was purified by preparative LCMS (Waters SunFire™ C18 column, 19 mm×100 mm, 5 μm particle size
  3. washeluting with a gradient of MeCN/water containing 0.1% NH4OH, at flow rate of 30 mL/min.)

출처 및 근거

ORD 기록
ord-ff5feaa540ba402b96d56f400f66a9b6
출처 데이터셋
uspto-grants-2015_12
특허 번호
US09200004B2

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