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Boron tribromide → HCID 57962136, Verbindung

HRID 542034
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 542034
[Cl:1][C:2]1[C:3]2[NH:4][C:5]3[CH:6]=[C:7]4[C:11](=[C:12]([CH:26]=3)[CH2:13][CH2:14][C:15]3[CH:25]=[C:19]([NH:20][C:21]([N:24]=2)=[N:22][CH:23]=1)[CH:18]=[CH:17][CH:16]=3)[O:10][C:9](=[O:27])[N:8]4[CH2:28][C:29]([O:31]C)=[O:30].B(Br)(Br)Br>ClCCl>[Cl:1][C:2]1[C:3]2[NH:4][C:5]3[CH:6]=[C:7]4[C:11](=[C:12]([CH:26]=3)[CH2:13][CH2:14][C:15]3[CH:25]=[C:19]([NH:20][C:21]([N:24]=2)=[N:22][CH:23]=1)[CH:18]=[CH:17][CH:16]=3)[O:10][C:9](=[O:27])[N:8]4[CH2:28][C:29]([OH:31])=[O:30]
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 2

HCID 25134Boron tribromide3×HCID 57962467HCID 57962467, Verbindung

Produkt 1

HCID 57962136HCID 57962136, VerbindungAusbeute 67,2 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6344DichloromethaneLösungsmittel4×

Reaktionsbedingungen

Temperatur
20 °C

Versuchsvorschrift

A solution of methyl [4-chloro-19-oxo-18-oxa-2,6,8,20,25-pentaazapentacyclo[14.6.1.1(3,7).1(9,13).0(17,21)]pentacosa-1(23),3(25),4,6,9(24),10,12,16,21-nonaen-20-yl]acetate (0.23 g, 0.51 mmol) in dichloromethane (15 mL) at −78° C. was treated with 1 M of boron tribromide in dichloromethane (1.5 mL, 1.5 mmol) and stirred at 20° C. for 16 h. The reaction mixture was cooled to 0° C., treated with additional 1 M of boron tribromide in dichloromethane (1.5 mL, 1.5 mmol), and stirred at 20° C. for 6 h. The reaction mixture was cooled to 0° C., quenched with 0.5 M HCl (10 mL) dropwise, concentrated and filtered. The brown solid that was collected was washed with water and dried. This material was diluted with dichloromethane (20 mL), cooled to 0° C., treated with 1 M of boron tribromide in dichloromethane (1.5 mL, 1.5 mmol), and stirred at 20° C. for 24 h. The reaction mixture was cooled to 0° C., quenched with 0.5 M HCl (10 mL) dropwise, concentrated and filtered. The brown solid that was collected was washed with water and dried to give the desired product (0.15 g, 67%) as a tan solid. LCMS for C21H17ClN5O4 (M+H)+: m/z=438.0.

Aufarbeitung

  1. temperatureThe reaction mixture was cooled to 0° C.
  2. stirringstirred at 20° C. for 6 h
  3. temperatureThe reaction mixture was cooled to 0° C.
  4. customquenched with 0.5 M HCl (10 mL) dropwise
  5. concentrationconcentrated
  6. filtrationfiltered
  7. customThe brown solid that was collected
  8. washwas washed with water
  9. customdried
  10. additionThis material was diluted with dichloromethane (20 mL)
  11. temperaturecooled to 0° C.
  12. stirringstirred at 20° C. for 24 h
  13. temperatureThe reaction mixture was cooled to 0° C.
  14. customquenched with 0.5 M HCl (10 mL) dropwise
  15. concentrationconcentrated
  16. filtrationfiltered
  17. customThe brown solid that was collected
  18. washwas washed with water
  19. customdried

Quellen und Nachweise

ORD-Eintrag
ord-e48f2e58f75a4f6ea8db08149fa4016f
Quelldatensatz
uspto-grants-2014_10
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08871753B2

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