Water → N-(4-(Chlorodifluoromethoxy)phenyl)-6-(3-hydroxyazetidin-1-yl)-5-(1H-pyrazol-5-yl)nicotinamide

HRID 525730노트

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HRID 525730 반응식
Cl.[OH:2][CH:3]1[CH2:6][NH:5][CH2:4]1.CCN(C(C)C)C(C)C.Cl[C:17]1[C:36]([C:37]2[NH:41][N:40]=[CH:39][CH:38]=2)=[CH:35][C:20]([C:21]([NH:23][C:24]2[CH:29]=[CH:28][C:27]([O:30][C:31]([Cl:34])([F:33])[F:32])=[CH:26][CH:25]=2)=[O:22])=[CH:19][N:18]=1.O>CC(O)C>[Cl:34][C:31]([F:32])([F:33])[O:30][C:27]1[CH:26]=[CH:25][C:24]([NH:23][C:21](=[O:22])[C:20]2[CH:35]=[C:36]([C:37]3[NH:41][N:40]=[CH:39][CH:38]=3)[C:17]([N:5]3[CH2:6][CH:3]([OH:2])[CH2:4]3)=[N:18][CH:19]=2)=[CH:29][CH:28]=1

참가 물질

6

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온도
140 °C

실험 절차

3-Hydroxyazetidine hydrochloride (53.2 mg, 0.486 mmol) and DIPEA (0.170 mL, 0.972 mmol) were added to a suspension of 6-chloro-N-(4-(chlorodifluoromethoxy)phenyl)-5-(1H-pyrazol-5-yl)nicotinamide (Stage 48.1, 100 mg, 0.243 mmol) in iPrOH (0.5 mL) and the RM was heated at 140° C. for 3 h. The RM was treated with water, extracted with EtOAc, and the combined extracts were dried over Na2SO4 and the solvent was evaporated off under reduced pressure to give. the crude product which was purified by flash chromatography (RediSep® Silica gel column, 24 g, DCM/MeOH 9:1) to give the title product as a yellow foam. HPLC (Condition 7) tR=5.518 min, UPLC-MS (Condition 3) tR=0.89 min, m/z=436 [M+H]+; 1H-NMR (400 MHz, DMSO-d6) δ ppm 3.49-3.57 (m, 2H) 3.87-3.99 (m, 2H) 4.32-4.44 (m, 1H) 5.53 (br.s, 1H) 6.40 (br.s, 1H) 7.33 (d, J=8.60 Hz, 2H) 7.81-7.91 (m, 3H) 8.06 (d, J=2.35 Hz, 1H) 8.70 (br.s, 1H) 10.23 (s, 1H) 13.01 (s, 1H).

후처리

  1. extractionextracted with EtOAc
  2. dry with materialthe combined extracts were dried over Na2SO4
  3. customthe solvent was evaporated off under reduced pressure
  4. customto give
  5. customthe crude product which was purified by flash chromatography (RediSep® Silica gel column, 24 g, DCM/MeOH 9:1)

출처 및 근거

ORD 기록
ord-a1b26e148438417a8898cfd5125d4982
출처 데이터셋
uspto-grants-2016_05
특허 번호
US09340537B2

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