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Trifluoroacetic acid → 4-((3S,4S)-3-Amino-4-hydroxypyrrolidin-1-yl)-N-(4-(chlorodifluoromethoxy)phenyl)-3-(1H-pyrazol-5-yl)benzamide

HRID 525751
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HRID 525751 반응식
O1CCCCC1[N:7]1[C:11](B2OC(C)(C)C(C)(C)O2)=[CH:10][CH:9]=[N:8]1.[NH2:21][C@@H:22]1[C@@H:26]([OH:27])[CH2:25][N:24]([C:28]2[CH:47]=[CH:46][C:31]([C:32]([NH:34][C:35]3[CH:40]=[CH:39][C:38]([O:41][C:42]([Cl:45])([F:44])[F:43])=[CH:37][CH:36]=3)=[O:33])=[CH:30][C:29]=2Br)[CH2:23]1.C([O-])([O-])=O.[Na+].[Na+].C(O)(C(F)(F)F)=O>COCCOC>[NH2:21][C@@H:22]1[C@@H:26]([OH:27])[CH2:25][N:24]([C:28]2[CH:29]=[CH:30][C:31]([C:32]([NH:34][C:35]3[CH:36]=[CH:37][C:38]([O:41][C:42]([Cl:45])([F:43])[F:44])=[CH:39][CH:40]=3)=[O:33])=[CH:46][C:47]=2[C:11]2[NH:7][N:8]=[CH:9][CH:10]=2)[CH2:23]1
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참가 물질

6

반응물 4

HCID 6422Trifluoroacetic acidHCID 10340Sodium CarbonateHCID 115872081-(tetrahydro-2H-pyran-2-yl)-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazoleHCID 899064294-((3 S,4S)-3-amino-4-hydroxypyrrolidin-1-yl)-3-bromo-N-(4-(chlorodifluoromethoxy)phenyl)benzamide

생성물 1

HCID 1180450264-((3S,4S)-3-Amino-4-hydroxypyrrolidin-1-yl)-N-(4-(chlorodifluoromethoxy)phenyl)-3-(1H-pyrazol-5-yl)benzamide

시약·촉매·용매 1

HCID 80711,2-Dimethoxyethane용매

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온도
80 °C

실험 절차

1-(Tetrahydro-2H-pyran-2-yl)-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole (82 mg, 0.288 mmol) and PdCl2(dppf)-(CH2Cl2) (10.07 mg, 12 μmol) were added to a mixture of 4-((3S,4S)-3-amino-4-hydroxypyrrolidin-1-yl)-3-bromo-N-(4-(chlorodifluoromethoxy)phenyl)benzamide (Stage 76.1, 100 mg, 0.206 mmol), Na2CO3 (0.308 mL, 0.617 mmol) in DME (2 mL) under argon atmosphere and the RM was heated at 80° C. for 4 h. The RM was filtered through Hyflo® and the solvent was evaporated off under reduced pressure to give a residue which was purified by flash chromatography (Silica gel column, 12 g, DCM/EtOH from 98:2 to 8:2). The resulting intermediate was dissolved in DCM (2 mL), treated with TFA (0.198 mL, 2.57 mmol) and the RM was stirred for RT for 3 h. The solvent was evaporated off under reduced pressure and the residue was treated with sat. aq. Na2CO3, and extracted with EtOAc. The combined extracts were washed with brine (20 mL), dried over Na2SO4 and the solvent was evaporated off under reduced pressure to give the crude product which was purified by flash chromatography (Silica gel column, 12 g, DCM/MeOH from 95:5 to 7:3) and crystallized from n-hexane/DCM to give the title product as a beige solid. HPLC (Condition 7) tR=5.774 min, UPLC-MS (Condition 3) tR=0.77 min, m/z=464.2 [M+H]+; 1H-NMR (400 MHz, DMSO-d6) δ ppm 2.73-2.99 (m, 2H) 3.22-3.44 (m, 3H) 3.93-4.04 (m, 1H) 5.33 (br. s, 1H) 6.39 (s, 1H) 6.74-6.94 (m, 1H) 7.31 (d, J=8.60 Hz, 2H) 7.76-8.03 (m, 4H) 10.17 (br. s, 1H).

후처리

  1. filtrationThe RM was filtered through Hyflo®
  2. customthe solvent was evaporated off under reduced pressure
  3. customto give a residue which
  4. customwas purified by flash chromatography (Silica gel column, 12 g, DCM/EtOH from 98:2 to 8:2)
  5. dissolutionThe resulting intermediate was dissolved in DCM (2 mL)
  6. customThe solvent was evaporated off under reduced pressure
  7. additionthe residue was treated with sat. aq. Na2CO3
  8. extractionextracted with EtOAc
  9. washThe combined extracts were washed with brine (20 mL)
  10. dry with materialdried over Na2SO4
  11. customthe solvent was evaporated off under reduced pressure
  12. customto give the crude product which
  13. customwas purified by flash chromatography (Silica gel column, 12 g, DCM/MeOH from 95:5 to 7:3)
  14. customcrystallized from n-hexane/DCM

출처 및 근거

ORD 기록
ord-9ebbe338fe2b4dfc930b970df00bb44f
출처 데이터셋
uspto-grants-2016_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09340537B2

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