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Hydrochloric Acid → HCID 58547920, Verbindung

HRID 2207799
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 2207799
[Cl:1][C:2]1[C:3]([O:8][CH:9]2[CH2:12][N:11](C(OC(C)(C)C)=O)[CH2:10]2)=[N:4][CH:5]=[CH:6][N:7]=1.Cl.O1CCOCC1>C(Cl)Cl>[NH:11]1[CH2:10][CH:9]([O:8][C:3]2[C:2]([Cl:1])=[N:7][CH:6]=[CH:5][N:4]=2)[CH2:12]1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 3

HCID 313Hydrochloric AcidHCID 312751,4-DioxaneHCID 585477833-(3-Chloro-pyrazin-2-yloxy)-azetidine-1-carboxylic acid tert-butyl ester

Produkt 1

HCID 58547920HCID 58547920, VerbindungAusbeute 62,6 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6344DichloromethaneLösungsmittel

Versuchsvorschrift

To a solution of tert-butyl 3-(3-chloropyrazin-2-yloxy)azetidine-1-carboxylate (see PREPARATION P20.2; 4.3 g, 15.05 mmol) and DCM (50 mL) was added 4M HCl in dioxane (3.76 mL, 15.05 mmol). After 72 hours, a precipitate coated the walls of the flask. The liquid was carefully decanted off and the rinsed with DCM (20 mL) and again carefully decanted off. The precipitate coated round bottomed flask was treated with DCM:saturated NaHCO3 (1:1, 150 mL). The aqueous layer was extracted with 10% MeOH in DCM (4×25 mL). The combined organic layers were concentrated in vacuo to give crude product. The aqueous layer still contained the majority of the product. The aqueous layer was concentrated in vacuo and the solids stirred with 10% MeOH in DCM (200 mL) for 2 hours, then filtered. The filtrate was concentrated in vacuo to give more crude product. The separate lots of crude product were combined to give crude 2-(azetidin-3-yloxy)-3-chloropyrazine (1.75 g, 62.6% yield), as a tan solid. The product was carried forward in the next step without further purification. MS (ESI) m/z 186.1 (MH+).

Aufarbeitung

  1. customThe liquid was carefully decanted off
  2. washthe rinsed with DCM (20 mL)
  3. customagain carefully decanted off
  4. additionThe precipitate coated round bottomed flask was treated with DCM
  5. extractionThe aqueous layer was extracted with 10% MeOH in DCM (4×25 mL)
  6. concentrationThe combined organic layers were concentrated in vacuo
  7. customto give crude product
  8. concentrationThe aqueous layer was concentrated in vacuo
  9. filtrationfiltered
  10. concentrationThe filtrate was concentrated in vacuo
  11. customto give more crude product

Quellen und Nachweise

ORD-Eintrag
ord-83f86029d3ef4ef3b064cab3038005b3
Quelldatensatz
uspto-grants-2016_06
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US09376450B2

Notizen zur Reaktion

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