Ethyl propiolate → pyrrolo[2,1-b]thiazole-7-carboxylic Acid Ethyl Ester

HRID 560324Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 560324
F[C:2](F)(F)S(OC[Si](C)(C)C)(=O)=O.CS[C:16]1[S:17][CH:18]=[CH:19][N:20]=1.[CH2:21]([O:23][C:24](=[O:27])[C:25]#[CH:26])[CH3:22].[F-].[Cs+]>CC#N>[CH2:21]([O:23][C:24]([C:25]1[CH:26]=[CH:2][N:20]2[CH:19]=[CH:18][S:17][C:16]=12)=[O:27])[CH3:22]

Komponenten

6

Versuchsvorschrift

Under nitrogen atmosphere (trimethylsilyl)methyl trifluoromethanesulfonate (16.3 mmol) is added dropwise to a mixture of 2-methylthio-1,3-thiazole (15.5 mmol) in MeCN (75 mL). The mixture is treated with propynoic acid ethyl ester (23.2 mmol), kept with occasional shaking for 30 min at RT and added dropwise to a vigorously stirred solution of CsF (21.7 mmol) and propynoic acid ethyl ester (23.2 mmol) in MeCN (75 mL). After stirring for 1 h the mixture is concentrated in vacuo, diluted with DCM (100 mL), washed twice with water and twice with brine and dried over Na2SO4. The solvents are removed in vacuo and the residue is purified by FC (gradient: heptane to heptane/EtOAc 8/2) to give the desired product.

Aufarbeitung

  1. stirringAfter stirring for 1 h the mixture
  2. concentrationis concentrated in vacuo
  3. additiondiluted with DCM (100 mL)
  4. washwashed twice with water and twice with brine
  5. dry with materialdried over Na2SO4
  6. customThe solvents are removed in vacuo
  7. customthe residue is purified by FC (gradient: heptane to heptane/EtOAc 8/2)

Quellen und Nachweise

ORD-Eintrag
ord-b73147700ce44246a1bc6cbff918ae67
Quelldatensatz
uspto-grants-2011_11
Patentnummer
US08063099B2

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