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Acetic Acid → 5-(1-isopropyl-piperidin-4-yl)-1-(toluene-4-sulfonyl)-1H-indole-2-carboxylic acid ethyl ester

HRID 74476
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 74476
Cl.[CH2:2]([O:4][C:5]([C:7]1[N:8]([S:22]([C:25]2[CH:30]=[CH:29][C:28]([CH3:31])=[CH:27][CH:26]=2)(=[O:24])=[O:23])[C:9]2[C:14]([CH:15]=1)=[CH:13][C:12]([CH:16]1[CH2:21][CH2:20][NH:19][CH2:18][CH2:17]1)=[CH:11][CH:10]=2)=[O:6])[CH3:3].C(N(CC)CC)C.[CH3:39][C:40]([CH3:42])=O.C(O)(=O)C.C(O[BH-](OC(=O)C)OC(=O)C)(=O)C.[Na+].C(=O)(O)[O-].[Na+]>ClC(Cl)C>[CH2:2]([O:4][C:5]([C:7]1[N:8]([S:22]([C:25]2[CH:26]=[CH:27][C:28]([CH3:31])=[CH:29][CH:30]=2)(=[O:23])=[O:24])[C:9]2[C:14]([CH:15]=1)=[CH:13][C:12]([CH:16]1[CH2:21][CH2:20][N:19]([CH:40]([CH3:42])[CH3:39])[CH2:18][CH2:17]1)=[CH:11][CH:10]=2)=[O:6])[CH3:3]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

8

Edukt 6

HCID 176Acetic AcidHCID 180AcetoneHCID 8471TriethylamineHCID 516892Sodium BicarbonateHCID 5049666Sodium triacetoxyborohydrideHCID 680052465-piperidin-4-yl-1-(toluene-4-sulfonyl)-1H-indole-2-carboxylic acid ethyl ester hydrochloride

Produkt 1

HCID 68005217
5-(1-isopropyl-piperidin-4-yl)-1-(toluene-4-sulfonyl)-1H-indole-2-carboxylic acid ethyl ester

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 63651,1-DichloroethaneLösungsmittel

Versuchsvorschrift

A mixture of 5-piperidin-4-yl-1-(toluene-4-sulfonyl)-1H-indole-2-carboxylic acid ethyl ester hydrochloride (253 mg, 0.592 mmol) in dichloroethane (4 ml), triethylamine (0.17 ml, 1.18 mmol), acetone (1.44 ml, 19.6 mmol), acetic acid (0.28 ml, 4.89 mmol), and sodium triacetoxyborohydride (318 mg, 1.50 mmol) was stirred at room temperature for 14.5 hours. The pH of the reaction mixture was adjusted to 9 (basic) using an aqueous solution saturated with sodium bicarbonate. The mixture was extracted with ethyl acetate. The extract was washed with an aqueous solution saturated with sodium chloride, and then dried over anhydrous sodium sulfate. The desiccant was removed by filtration, and concentration was performed. The resulting residue was purified by amino gel column chromatography (hexane/ethyl acetate=92/8 to 35/65). Thus, 5-(1-isopropyl-piperidin-4-yl)-1-(toluene-4-sulfonyl)-1H-indole-2-carboxylic acid ethyl ester was obtained as a colorless gum-like material (191 mg, 69%).

Aufarbeitung

  1. extractionThe mixture was extracted with ethyl acetate
  2. washThe extract was washed with an aqueous solution saturated with sodium chloride
  3. dry with materialdried over anhydrous sodium sulfate
  4. customThe desiccant was removed by filtration, and concentration
  5. customThe resulting residue was purified by amino gel column chromatography (hexane/ethyl acetate=92/8 to 35/65)

Quellen und Nachweise

ORD-Eintrag
ord-1d42c6a62ba648a69c404144ffb5b899
Quelldatensatz
uspto-grants-2014_09
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08829199B2

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