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Cesium carbonate → (1R,2R)-2-({4'-[(6-Chloro-1,3-benzothiazol-2-yl)amino]-3'-fluoro-1,1'-biphenyl-4-yl}carbonyl)cyclopentanecarboxylic acid

HRID 9610
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 9610
I[C:2]1[CH:7]=[CH:6][C:5]([NH:8][C:9]2[S:10][C:11]3[CH:17]=[C:16]([Cl:18])[CH:15]=[CH:14][C:12]=3[N:13]=2)=[C:4]([F:19])[CH:3]=1.B1(B2OC(C)(C)C(C)(C)O2)OC(C)(C)C(C)(C)O1.CC([O-])=O.[K+].Br[C:44]1[CH:59]=[CH:58][C:47]([C:48]([C@@H:50]2[CH2:54][CH2:53][CH2:52][C@H:51]2[C:55]([OH:57])=[O:56])=[O:49])=[CH:46][CH:45]=1.C([O-])([O-])=O.[Cs+].[Cs+]>CN(C=O)C.O.C1C=CC(P(C2C=CC=CC=2)[C-]2C=CC=C2)=CC=1.C1C=CC(P(C2C=CC=CC=2)[C-]2C=CC=C2)=CC=1.Cl[Pd]Cl.[Fe+2]>[Cl:18][C:16]1[CH:15]=[CH:14][C:12]2[N:13]=[C:9]([NH:8][C:5]3[CH:6]=[CH:7][C:2]([C:44]4[CH:45]=[CH:46][C:47]([C:48]([C@@H:50]5[CH2:54][CH2:53][CH2:52][C@H:51]5[C:55]([OH:57])=[O:56])=[O:49])=[CH:58][CH:59]=4)=[CH:3][C:4]=3[F:19])[S:10][C:11]=2[CH:17]=1
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

9

Edukt 5

HCID 10796Cesium carbonateHCID 517044Potassium AcetateHCID 2733548Bis(pinacolato)diboraneHCID 23549251trans-2-(4-Bromobenzoyl)cyclopentanecarboxylic acidHCID 23549325N-(4-Iodo-2-fluorophenyl)-6-chloro-1,3-benzothiazol-2-amine

Produkt 1

HCID 11466071
(1R,2R)-2-({4'-[(6-Chloro-1,3-benzothiazol-2-yl)amino]-3'-fluoro-1,1'-biphenyl-4-yl}carbonyl)cyclopentanecarboxylic acid
Ausbeute 60 %

Reagenzien, Katalysatoren, Lösungsmittel 3

HCID 44119782Bis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)Katalysator2×HCID 962WaterLösungsmittelHCID 6228DimethylformamideLösungsmittel

Reaktionsbedingungen

Temperatur
85 °C

Versuchsvorschrift

A suspension of N-(4-iodo-2-fluorophenyl)-6-chloro-1,3-benzothiazol-2-amine (200 mg, 0.49 mmol), bis(pinacolato)diboron (130 mg, 0.52 mmol), KOAc (150 mg, 1.48 mmol), and PdCl2(dppf) (30 mg, 0.04 mmol) in DMF (5.0 mL) was degassed by bubbling a flow of nitrogen for 30 minutes. The reaction mixture was heated under nitrogen at 85° C. for 3 h. After the mixture was cooled to rt, (1R,2R)-2-(4-bromobenzoyl)cyclopentanecarboxylic acid (140 mg, 0.49 mmol, >99% ee), Cs2CO3 (400 mg, 1.23 mmol) and PdCl2(dppf) (30 mg, 0.04 mmol) were added, and the reaction mixture was heated at 85° C. under nitrogen for 3 h. TLC analysis showed little starting materials remaining. The reaction mixture was cooled to rt, and diluted with water (50 mL). After the mixture was filtered through a pad of Celite®, 1 N HCl was added to the filtrate to adjust the acidity to pH<3. The solid that formed was collected by filtration, then dissolved in EtOAc (50 mL), and the resulting solution was dried over Na2SO4. Removal of solvent and drying in vacuo provided the desired product (120 mg, 60%, >99% ee). LC-MS m/z 495.3 (MH+), retention time 4.01 min.

Aufarbeitung

  1. customwas degassed
  2. customby bubbling a flow of nitrogen for 30 minutes
  3. temperatureAfter the mixture was cooled to rt
  4. temperaturethe reaction mixture was heated at 85° C. under nitrogen for 3 h
  5. temperatureThe reaction mixture was cooled to rt
  6. filtrationAfter the mixture was filtered through a pad of Celite®, 1 N HCl
  7. additionwas added to the filtrate
  8. customThe solid that formed
  9. filtrationwas collected by filtration
  10. dissolutiondissolved in EtOAc (50 mL)
  11. dry with materialthe resulting solution was dried over Na2SO4
  12. customRemoval of solvent
  13. customdrying in vacuo

Quellen und Nachweise

ORD-Eintrag
ord-947301e8b5bd42b680eea3d2d619713c
Quelldatensatz
uspto-grants-2006_08
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07091228B2

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