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Formamide → HCID 178461168, Verbindung

HRID 82396
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Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 82396
[NH2:1][C:2]1[CH2:6][CH2:5][C@@H:4]([CH3:7])[C:3]=1[C:8]([O:10]CC)=O.C([O-])=O.[NH4+].[CH:17]([NH2:19])=O>>[CH3:7][C@H:4]1[C:3]2[C:8]([OH:10])=[N:19][CH:17]=[N:1][C:2]=2[CH2:6][CH2:5]1
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 3

HCID 713FormamideHCID 2723923Ammonium formateHCID 59671147Ethyl (5R)-2-amino-5-methyl-1-cyclopentene-1-carboxylate

Produkt 1

HCID 178461168HCID 178461168, VerbindungAusbeute 65 %

Reaktionsbedingungen

Temperatur
150 °C

Versuchsvorschrift

A solution containing (R)-ethyl 2-amino-5-methylcyclopent-1-enecarboxylate (161.61 g, 955.024 mmol) and ammonium formate (90.3298 g, 1432.54 mmol) in formamide (303.456 mL, 7640.19 mmol) was heated to an internal temperature of 150° C. and stirred for 17 hours. The reaction mixture was cooled and transferred to a 2L single nextracted flask. The excess formamidine was removed by high vacuum distillation. Once formamidine stopped coming over, the remaining oil in the still pot was dissolved in DCM and washed with brine (3×200 mL). The combined aqueous portions were extracted with DCM (1×). The combined organic extracts were dried (Na2SO4), filtered, and concentrated. The resulting brown oil was dissolved in minimal DCM, and this solution was added using a separatory funnel to a stirred solution of ether (ca. 5 volumes of ether vs. DCM solution). This caused some brown precipitate to form. This brown precipitate was removed by filtration through a medium frit funnel, which was rinsed with ether and disposed. The filtrate was concentrated. The trituration from ether repeated two more times and then dried on high vacuum line to give (R)-5-methyl-6,7-dihydro-5H-cyclopenta[d]pyrimidin-4-ol (93.225 g, 65.00% yield) as a brown-yellow pasty solid. LC/MS (APCI−) m/z 149.2.

Aufarbeitung

  1. temperatureThe reaction mixture was cooled
  2. customThe excess formamidine was removed by high vacuum distillation
  3. dissolutionpot was dissolved in DCM
  4. washwashed with brine (3×200 mL)
  5. extractionThe combined aqueous portions were extracted with DCM (1×)
  6. dry with materialThe combined organic extracts were dried (Na2SO4)
  7. filtrationfiltered
  8. concentrationconcentrated
  9. dissolutionThe resulting brown oil was dissolved in minimal DCM
  10. additionthis solution was added
  11. customto form
  12. customThis brown precipitate was removed by filtration through a medium frit funnel
  13. washwhich was rinsed with ether
  14. concentrationThe filtrate was concentrated
  15. customdried on high vacuum line

Quellen und Nachweise

ORD-Eintrag
ord-99883e55fead44cb8ee166b5c91bd365
Quelldatensatz
uspto-grants-2014_09
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08846681B2

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