Boron tribromide → 4-[3-(4-Chloro-phenyl)-5,6,7,8-tetrahydro-4H-1,2,6-triaza-azulen-1-ylmethyl]-2-fluoro-phenol

HRID 749799Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 749799
B(Br)(Br)Br.[Cl:5][C:6]1[CH:11]=[CH:10][C:9]([C:12]2[C:21]3[CH2:20][CH2:19][NH:18][CH2:17][CH2:16][C:15]=3[N:14]([CH2:22][C:23]3[CH:28]=[CH:27][C:26]([O:29]C)=[C:25]([F:31])[CH:24]=3)[N:13]=2)=[CH:8][CH:7]=1>C(Cl)Cl>[Cl:5][C:6]1[CH:11]=[CH:10][C:9]([C:12]2[C:21]3[CH2:20][CH2:19][NH:18][CH2:17][CH2:16][C:15]=3[N:14]([CH2:22][C:23]3[CH:28]=[CH:27][C:26]([OH:29])=[C:25]([F:31])[CH:24]=3)[N:13]=2)=[CH:8][CH:7]=1

Komponenten

4

Edukt 2

HCID 25134Boron tribromideHCID 597526763-(4-Chloro-phenyl)-1-(3-fluoro-4-methoxy-benzyl)-1,4,5,6,7,8-hexahydro-1,2,6-triaza-azulene

Produkt 1

HCID 117490654-[3-(4-Chloro-phenyl)-5,6,7,8-tetrahydro-4H-1,2,6-triaza-azulen-1-ylmethyl]-2-fluoro-phenolAusbeute 75,5 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6344DichloromethaneLösungsmittel

Versuchsvorschrift

BBr3 (0.13 mL) was added slowly to a 0° C. solution of 0.022 g of 3-(4-chloro-phenyl)-1-(3-fluoro-4-methoxy-benzyl)-1,4,5,6,7,8-hexahydro-1,2,6-triaza-azulene (Example 96) in CH2Cl2 (20 mL). After 1 h, the mixture was warmed to RT and stirred for 18 h. The reaction was then cooled back to 0° C. and quenched by the addition of 5 mL of satd. aq. NaHCO3. The aqueous layer was extracted with methanolic CH2Cl2 (2×). The combined organic layers were dried over Na2SO4 and concentrated. The crude oil was purified by preparative TLC (9:1 CH2Cl2/2 M NH3 in MeOH) to afford the title compound (0.016 g) as a tan solid. MS (ESI): exact mass calculated for C20H19ClFN3O, 371.12; found, m/z 372.1 [M+H]+. 1H NMR (400 MHz, CD3OD): 7.50-7.42 (m, 4H), 6.86-6.79 (m, 3H), 5.26 (s, 2H), 3.31-3.26 (m, 2H), 2.96-2.95 (m, 4H), 2.90-2.87 (m, 2H), 2.81-2.79 (m, 2H). 13C NMR (100 MHz, CD3OD): 154.2, 151.8, 149.6, 146.1, 146.0, 143.8, 134.8, 133.4, 131.1, 130.3, 130.2, 129.7, 124.0, 119.1, 115.6, 115.4, 53.1, 50.4, 29.0, 27.5.

Aufarbeitung

  1. temperatureThe reaction was then cooled back to 0° C.
  2. customquenched by the addition of 5 mL of satd
  3. extractionThe aqueous layer was extracted with methanolic CH2Cl2 (2×)
  4. dry with materialThe combined organic layers were dried over Na2SO4
  5. concentrationconcentrated
  6. customThe crude oil was purified by preparative TLC (9:1 CH2Cl2/2 M NH3 in MeOH)

Quellen und Nachweise

ORD-Eintrag
ord-15ac02305e7543f3ac2b171df5b24625
Quelldatensatz
uspto-grants-2008_07
Patentnummer
US07402680B2

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