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3-Aminoisonicotinaldehyde → HCID 68243919, Verbindung

HRID 588406
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 588406
[NH2:1][C:2]1[CH:3]=[N:4][CH:5]=[CH:6][C:7]=1[CH:8]=O.Cl.[F:11][C:12]1([F:17])[CH2:16][CH2:15][NH:14][CH2:13]1.[BH-](OC(C)=O)(OC(C)=O)OC(C)=O.[Na+]>C(Cl)Cl.CO>[F:11][C:12]1([F:17])[CH2:16][CH2:15][N:14]([CH2:8][C:7]2[CH:6]=[CH:5][N:4]=[CH:3][C:2]=2[NH2:1])[CH2:13]1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 3

HCID 27630013-AminoisonicotinaldehydeHCID 5049666Sodium triacetoxyborohydrideHCID 249034823,3-Difluoropyrrolidine hydrochloride

Produkt 1

HCID 68243919HCID 68243919, VerbindungAusbeute 56,3 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 887MethanolLösungsmittel
HCID 6344
Dichloromethane
Lösungsmittel

Versuchsvorschrift

3-Amino-pyridine-4-carbaldehyde (250 mg, 2.05 mmol) was dissolved in DCM (4 mL) and MeOH (4 mL), and 3,3-difluoropyrrolidine hydrochloride (353 mg, 2.46 mmol) and NaBH(OAc)3 (521 mg, 2.46 mmol) were added. The reaction mixture was stirred for 18 h, quenched with water (5 mL) and the solvents were removed in vacuo. The residue was dissolved in DCM (20 mL) and washed with sat aq Na2CO3 (5 mL). The aqueous phase was extracted with DCM (3×20 mL) and the combined organic fractions were dried (MgSO4) and concentrated in vacuo to give the crude title compound as a yellow gum (246 mg, 56%). LCMS (ES+): 214.0 (M+H)+.

Aufarbeitung

  1. customquenched with water (5 mL)
  2. customthe solvents were removed in vacuo
  3. dissolutionThe residue was dissolved in DCM (20 mL)
  4. washwashed
  5. extractionThe aqueous phase was extracted with DCM (3×20 mL)
  6. dry with materialthe combined organic fractions were dried (MgSO4)
  7. concentrationconcentrated in vacuo

Quellen und Nachweise

ORD-Eintrag
ord-bf5b6fb9e2b2478a96a0d9d3b91c2996
Quelldatensatz
uspto-grants-2016_01
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US09227967B2

Notizen zur Reaktion

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