Diisopropylethylamine → 6-(4-Bromo-2-methyl-phenylamino)-7-fluoro-3-pent-4-enyl-3H-benzoimidazole-5-carboxylic acid cyclopropylmethoxy-amide

HRID 31987

Reaktionsgleichung

Reaktionsgleichung von HRID 31987
[Br:1][C:2]1[CH:7]=[CH:6][C:5]([NH:8][C:9]2[C:10]([C:24]([OH:26])=O)=[CH:11][C:12]3[N:16]([CH2:17][CH2:18][CH2:19][CH:20]=[CH2:21])[CH:15]=[N:14][C:13]=3[C:22]=2[F:23])=[C:4]([CH3:27])[CH:3]=1.CCN(C(C)C)C(C)C.C1CN([P+](ON2N=NC3C=[CH:58][CH:59]=[CH:60][C:55]2=3)(N2CCCC2)N2CCCC2)CC1.F[P-](F)(F)(F)(F)F.Cl.C1([N:74](C)[OH:75])CC1>C1COCC1.C(Cl)Cl.C(OCC)(=O)C>[CH:59]1([CH2:58][O:75][NH:74][C:24]([C:10]2[C:9]([NH:8][C:5]3[CH:6]=[CH:7][C:2]([Br:1])=[CH:3][C:4]=3[CH3:27])=[C:22]([F:23])[C:13]3[N:14]=[CH:15][N:16]([CH2:17][CH2:18][CH2:19][CH:20]=[CH2:21])[C:12]=3[CH:11]=2)=[O:26])[CH2:60][CH2:55]1

Komponenten

7

Edukt 4

HCID 81531DiisopropylethylamineHCID 2724699PyBOPHCID 211142136-(4-Bromo-2-methyl-phenylamino)-7-fluoro-3-pent-4-enyl-3H-benzoimidazole-5-carboxylic acidHCID 21114231Cyclopropyl methyl hydroxylamine hydrochloride

Produkt 1

HCID 588906146-(4-Bromo-2-methyl-phenylamino)-7-fluoro-3-pent-4-enyl-3H-benzoimidazole-5-carboxylic acid cyclopropylmethoxy-amideAusbeute 70 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 8857Ethyl AcetateLösungsmittelHCID 21919333Tetrahydrofurane dichloromethaneLösungsmittel

Versuchsvorschrift

6-(4-Bromo-2-methyl-phenylamino)-7-fluoro-3-pent-4-enyl-3H-benzoimidazole-5-carboxylic acid 10d (0.390 g, 0.902 mmol) is dissolved in 1:1 THF/methylene chloride (6 mL) and Hunig's base (0.346 mL, 1.985 mmol) is added followed by PyBOP (0.563 g, 1.083 mmol). After 10 minutes, cyclopropyl methyl hydroxylamine hydrochloride (0.134 g, 1.083 mmol) is added. After 16 hours, the reaction mixture is diluted with ethyl acetate and washed with 0.1 N HCl, saturated NaHCO3, and brine. The organic layer is dried (Na2SO4) and concentrated under reduced pressure. The crude yellow residue is purified by FCC eluted with ethyl acetate to give 0.315 g (70%) pure desired product as a yellow solid: MS APCI (+) m/z 503, 501 (M+1 Br pattern) detected.

Aufarbeitung

  1. additionis added
  2. waitAfter 16 hours
  3. washwashed with 0.1 N HCl, saturated NaHCO3, and brine
  4. dry with materialThe organic layer is dried (Na2SO4)
  5. concentrationconcentrated under reduced pressure
  6. customThe crude yellow residue is purified by FCC
  7. washeluted with ethyl acetate

Quellen und Nachweise

ORD-Eintrag
ord-1739a122365b48cdae3dd56d81855777
Quelldatensatz
uspto-grants-2008_09
Patentnummer
US07425637B2

Verknüpfte Notizen

Wird geladen…