4-Methylcyclohexane-1-carbonyl chloride → 5-(3,3-Dimethyl-but-1-ynyl)-3-[[2-(ethoxy-methyl-phosphinoyl)-ethyl]-(4-methyl-cyclohexanecarbonyl)-amino]-thiophene-2-carboxylic acid methyl ester

HRID 1614914Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1614914
[CH3:1][O:2][C:3]([C:5]1[S:6][C:7]([C:19]#[C:20][C:21]([CH3:24])([CH3:23])[CH3:22])=[CH:8][C:9]=1[NH:10][CH2:11][CH2:12][P:13]([O:16][CH2:17][CH3:18])([CH3:15])=[O:14])=[O:4].[CH3:25][CH:26]1[CH2:31][CH2:30][CH:29]([C:32](Cl)=[O:33])[CH2:28][CH2:27]1>N1C=CC=CC=1.CCOC(C)=O>[CH3:1][O:2][C:3]([C:5]1[S:6][C:7]([C:19]#[C:20][C:21]([CH3:23])([CH3:22])[CH3:24])=[CH:8][C:9]=1[N:10]([CH2:11][CH2:12][P:13]([O:16][CH2:17][CH3:18])([CH3:15])=[O:14])[C:32]([CH:29]1[CH2:30][CH2:31][CH:26]([CH3:25])[CH2:27][CH2:28]1)=[O:33])=[O:4]

Komponenten

5

Edukt 2

HCID 129863574-Methylcyclohexane-1-carbonyl chlorideHCID 670343375-(3,3-Dimethyl-but-1-ynyl)-3-[2-(ethoxy-methyl-phosphinoyl)-ethylamino]-thiophene-2-carboxylic acid methyl ester

Produkt 1

HCID 670337505-(3,3-Dimethyl-but-1-ynyl)-3-[[2-(ethoxy-methyl-phosphinoyl)-ethyl]-(4-methyl-cyclohexanecarbonyl)-amino]-thiophene-2-carboxylic acid methyl esterAusbeute 80,5 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 1049PyridineLösungsmittelHCID 8857Ethyl AcetateLösungsmittel

Reaktionsbedingungen

Temperatur
100 °C

Versuchsvorschrift

5-(3,3-Dimethyl-but-1-ynyl)-3-[2-(ethoxy-methyl-phosphinoyl)-ethylamino]-thiophene-2-carboxylic acid methyl ester (233 mg, 0.629 mmol) was dissolved in pyridine (4 mL) and then 4-methyl-cyclohexanecarbonyl chloride (506 mg, 3.15 mmol) was added. The reaction was stirred for 7 hours at 100° C., the heat to the oil bath was shut off and the reaction was allowed to stir for a further 9 hours. The reaction was diluted with EtOAc and extracted with H2O. The organic phase was then extracted with brine and dried over Na2SO4. The drying agent was removed by vacuum filtration and the filtrate was concentrated. 5-(3,3-Dimethyl-but-1-ynyl)-3-[[2-(ethoxy-methyl-phosphinoyl)-ethyl]-(4-methyl-cyclohexanecarbonyl)-amino]-thiophene-2-carboxylic acid methyl ester (251 mg, 78%) was isolated from the residue by silica gel column chromatography.

Aufarbeitung

  1. temperaturethe heat to the oil bath
  2. stirringto stir for a further 9 hours
  3. extractionextracted with H2O
  4. extractionThe organic phase was then extracted with brine
  5. dry with materialdried over Na2SO4
  6. customThe drying agent was removed by vacuum filtration
  7. concentrationthe filtrate was concentrated

Quellen und Nachweise

ORD-Eintrag
ord-f3453c449dbe4886a96a657d349ed864
Quelldatensatz
uspto-grants-2014_07
Patentnummer
US08765722B2

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