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Potassium Phosphate, Tribasic → {5-[1-(2-Morpholin-4-yl-ethyl)-1H-pyrazol-4-yl]-thiophen-3-yl}-(octahydro-quinolin-1yl)-methanone formate

HRID 1914559
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HRID 1914559 반응식
Br[C:2]1[S:6][CH:5]=[C:4]([C:7]([N:9]2[C@@H:18]3[C@@H:13]([CH2:14][CH2:15][CH2:16][CH2:17]3)[CH2:12][CH2:11][CH2:10]2)=[O:8])[CH:3]=1.CC1(C)C(C)(C)OB([C:27]2[CH:28]=[N:29][N:30]([CH2:32][CH2:33][N:34]3[CH2:39][CH2:38][O:37][CH2:36][CH2:35]3)[CH:31]=2)[O:21]1.C1(P(C2CCCCC2)C2CCCCC2)CCCCC1.P([O-])([O-])([O-])=O.[K+].[K+].[K+]>COCCOC.O.C1C=CC(/C=C/C(/C=C/C2C=CC=CC=2)=O)=CC=1.C1C=CC(/C=C/C(/C=C/C2C=CC=CC=2)=O)=CC=1.C1C=CC(/C=C/C(/C=C/C2C=CC=CC=2)=O)=CC=1.[Pd].[Pd]>[CH:7]([OH:8])=[O:21].[N:34]1([CH2:33][CH2:32][N:30]2[CH:31]=[C:27]([C:2]3[S:6][CH:5]=[C:4]([C:7]([N:9]4[CH:18]5[CH:13]([CH2:14][CH2:15][CH2:16][CH2:17]5)[CH2:12][CH2:11][CH2:10]4)=[O:8])[CH:3]=3)[CH:28]=[N:29]2)[CH2:35][CH2:36][O:37][CH2:38][CH2:39]1
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참가 물질

8

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HCID 62657Potassium Phosphate, TribasicHCID 75806TricyclohexylphosphineHCID 177499241-(2-Morpholinoethyl)-1H-pyrazole-4-boronic acid pinacol esterHCID 86646712HCID 86646712, 화합물

생성물 1

HCID 66850322{5-[1-(2-Morpholin-4-yl-ethyl)-1H-pyrazol-4-yl]-thiophen-3-yl}-(octahydro-quinolin-1yl)-methanone formate수율 67.9%

시약·촉매·용매 3

HCID 9811564Bis(dibenzylideneacetone)palladium촉매HCID 962Water용매HCID 80711,2-Dimethoxyethane용매

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온도
140 °C

실험 절차

cis-(5-Bromo-thiophen-3-yl)-(octahydro-quinolin-1-yl)-methanone (0.06 g, 0.18 mmol) was mixed with 4-{2-[4-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-pyrazol-1-yl]-ethyl}-morpholine (0.062 g, 0.2 mmol), tricyclohexylphosphine (0.004 g, 0.01 mmol), potassium phosphate (0.047 g, 0.22 mmol) and tris(dibenzylideneacetone)dipalladium (0) (0.007 g, 0.008 mmol) in DME (2 mL), IMS (0.5 mL) and water (0.25 mL). The reaction mixture was purged with argon then heated by microwave irradiation to 140° C. for 20 minutes. The resultant mixture was diluted with water and extracted with DCM (×2) then the organic phase was dried over sodium sulfate, filtered and the solvent evaporated. The residue was purified by HPLC, eluting with 10%-98% acetonitrile in water (0.1% formic acid) over 20 minutes. The fractions containing the desired product were freeze-dried to give the title compound (0.029 g). LCMS m/z 429.25 [M+H]+ R.T.=7.03 min (Analytical Method 2).

후처리

  1. customThe reaction mixture was purged with argon
  2. additionThe resultant mixture was diluted with water
  3. extractionextracted with DCM (×2)
  4. dry with materialthe organic phase was dried over sodium sulfate
  5. filtrationfiltered
  6. customthe solvent evaporated
  7. customThe residue was purified by HPLC
  8. washeluting with 10%-98% acetonitrile in water (0.1% formic acid) over 20 minutes
  9. additionThe fractions containing the desired product
  10. customwere freeze-dried

출처 및 근거

ORD 기록
ord-b2a321dab17648a79ee019247f1b7d5a
출처 데이터셋
uspto-grants-2013_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08614209B2

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