2-Methyl-3-butyn-2-ol → 4-Acetylamino-9-(3-hydroxy-3-methyl-but-1-ynyl)-4,5-dihydro-6-oxa-3-thia-1-aza-benzo[e]azulene-2-carboxylic acid methyl ester

HRID 575112Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 575112
[CH3:1][O:2][C:3]([C:5]1[S:6][C:7]2[CH:8]([NH:20][C:21](=[O:23])[CH3:22])[CH2:9][O:10][C:11]3[CH:18]=[CH:17][C:16](Br)=[CH:15][C:12]=3[C:13]=2[N:14]=1)=[O:4].C1C=CC(P(C2C=CC=CC=2)C2C=CC=CC=2)=CC=1.[CH3:43][C:44]([OH:48])([C:46]#[CH:47])[CH3:45]>CN(C=O)C.CC([O-])=O.CC([O-])=O.[Pd+2].[Cu]I>[CH3:1][O:2][C:3]([C:5]1[S:6][C:7]2[CH:8]([NH:20][C:21](=[O:23])[CH3:22])[CH2:9][O:10][C:11]3[CH:18]=[CH:17][C:16]([C:47]#[C:46][C:44]([OH:48])([CH3:45])[CH3:43])=[CH:15][C:12]=3[C:13]=2[N:14]=1)=[O:4]

Komponenten

7

Edukt 3

HCID 82582-Methyl-3-butyn-2-olHCID 11776TriphenylphosphineHCID 866931414-Acetylamino-9-bromo-4,5-dihydro-6-oxa-3-thia-1-aza-benzo[e]azulene-2-carboxylic acid methyl ester

Produkt 1

HCID 866931424-Acetylamino-9-(3-hydroxy-3-methyl-but-1-ynyl)-4,5-dihydro-6-oxa-3-thia-1-aza-benzo[e]azulene-2-carboxylic acid methyl esterAusbeute 45 %

Reagenzien, Katalysatoren, Lösungsmittel 3

HCID 24350Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)KatalysatorHCID 167845palladium(II) acetateKatalysatorHCID 6228DimethylformamideLösungsmittel

Reaktionsbedingungen

Temperatur
80 °C

Versuchsvorschrift

To a stirred mixture of 4-Acetylamino-9-bromo-4,5-dihydro-6-oxa-3-thia-1-aza-benzo[e]azulene-2-carboxylic acid methyl ester (180 mg, 0.453 mmol) in TEA (5 mL) and DMF (1 mL) were added Pd(OAc)2 (20.3 mg, 0.091 mmol), PPh3 (35.6 mg, 0.136 mmol), CuI (17.26 mg, 0.091 mmol) and 2-methylbut-3-yn-2-ol (190.6 mg, 2.266 mmol). The reaction mixture was degassed with N2 and heated in a microwave reactor at 80° C. for 2 h. Then the mixture was cooled to room temperature, and EtOAc was added. The mixture was filtered though Celite, and the filtrate was washed with saturated brine, dried over Na2SO4, filtered, concentrated in vacuo, and purified by flash column chromatography (silica gel, EtOAc in hexane from 10% to 20%) to afford 4-Acetylamino-9-(3-hydroxy-3-methyl-but-1-ynyl)-4,5-dihydro-6-oxa-3-thia-1-aza-benzo[e]azulene-2-carboxylic acid methyl ester (81 mg, 45%) as a light yellow solid. LC-MS (ESI & APCI): 399.1 (M−1).

Aufarbeitung

  1. customThe reaction mixture was degassed with N2
  2. temperatureThen the mixture was cooled to room temperature
  3. additionEtOAc was added
  4. filtrationThe mixture was filtered though Celite
  5. washthe filtrate was washed with saturated brine
  6. dry with materialdried over Na2SO4
  7. filtrationfiltered
  8. concentrationconcentrated in vacuo
  9. custompurified by flash column chromatography (silica gel, EtOAc in hexane from 10% to 20%)

Quellen und Nachweise

ORD-Eintrag
ord-359b9afd491342e2a388bd5018bff121
Quelldatensatz
uspto-grants-2015_05
Patentnummer
US09034866B2

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