Dimethylformamide → (R)-3-(N-Benzyloxycarbonylpyrrolidin-2-ylmethyl)-7-bromo-5-(methylaminosulfonylmethyl)-1H-indole

HRID 975031Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 975031
[CH2:1]([O:8][C:9]([N:11]1[CH2:15][CH2:14][CH2:13][C@@H:12]1[CH:16]=[CH:17][CH2:18][N:19]([C:26]1[C:31](Br)=[CH:30][C:29]([CH2:33][S:34]([NH:37][CH3:38])(=[O:36])=[O:35])=[CH:28][C:27]=1[Br:39])C(=O)C(F)(F)F)=[O:10])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.CN(C)C=O>C(N(CC)CC)C.[Cl-].C([N+](CCCC)(CCCC)CCCC)CCC.C([O-])(=O)C.[Pd+2].C([O-])(=O)C>[CH2:1]([O:8][C:9]([N:11]1[CH2:15][CH2:14][CH2:13][C@@H:12]1[CH2:16][C:17]1[C:31]2[C:26](=[C:27]([Br:39])[CH:28]=[C:29]([CH2:33][S:34]([NH:37][CH3:38])(=[O:35])=[O:36])[CH:30]=2)[NH:19][CH:18]=1)=[O:10])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1

Komponenten

6

Edukt 2

HCID 6228DimethylformamideHCID 53700037(R)-1-(N-Benzyloxycarbonylpyrrolidin-2-yl)-3-[N-(4-methylaminosulfonylmethyl-2,6-dibromophenyl)-N-trifluoroacetylamino]propene

Produkt 1

HCID 11038630(R)-3-(N-Benzyloxycarbonylpyrrolidin-2-ylmethyl)-7-bromo-5-(methylaminosulfonylmethyl)-1H-indole

Reagenzien, Katalysatoren, Lösungsmittel 3

HCID 70681Tetrabutylammonium ChlorideKatalysatorHCID 167845palladium(II) acetateKatalysatorHCID 8471TriethylamineLösungsmittel

Reaktionsbedingungen

Temperatur
80 °C

Versuchsvorschrift

(R)-1-(N-Benzyloxycarbonylpyrrolidin-2-yl)-3-[N-(4-methylaminosulfonylmethyl-2,6-dibromophenyl)-N-trifluoroacetylamino]propene (9.00 g) in triethylamine (70 mL) containing N,N-dimethylformamide (20 mL), tetra-n-butylammonium chloride (3.61 g) and palladium acetate (1.01 g) was heated at 80° C. until conversion was complete. The cooled reaction mixture was filtered through CELITE and washed with methylene chloride. The combined filtrate and washings were then evaporated in vacuo onto silica gel (15 g) then purified by column chromatography (SiO2--1.6 kg) eluted with 4% acetone in chloroform. The product-rich fractions were combined and evaporated then re-purified by crystallization from a mixture of diethyl ether (50 mL) and methylene chloride (10 mL). The title compound was recovered by filtration (washing with hexanes) as a colorless solid (2.40 g). TLC (methylene chloride/acetone 10:1) Rf=0.35; Anal calcd. for C23H26BrN3O4S: C, 53.1; H, 5.0; N, 8.1. Found C, 53.13; H, 5.0; N, 7.8.

Aufarbeitung

  1. customThe cooled reaction mixture
  2. filtrationwas filtered through CELITE
  3. washwashed with methylene chloride
  4. customThe combined filtrate and washings were then evaporated in vacuo onto silica gel (15 g)
  5. customthen purified by column chromatography (SiO2--1.6 kg)
  6. washeluted with 4% acetone in chloroform
  7. customevaporated
  8. customthen re-purified by crystallization from a mixture of diethyl ether (50 mL) and methylene chloride (10 mL)
  9. filtrationThe title compound was recovered by filtration (washing with hexanes) as a colorless solid (2.40 g)

Quellen und Nachweise

ORD-Eintrag
ord-4ecd9739a67d4d2eb326df629981f7bc
Quelldatensatz
uspto-grants-1997_03
Patentnummer
US05607951

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