StartseiteMCPWorkbenchSkills
StartseiteWorkbenchBenachrichtigungenMein Bereich
llms.txt · MCP-AnleitungDatenschutz · Nutzungsbedingungen · Supportv1.8.0
  1. Startseite
  2. /Reaktion

Pyridine → 3-Benzyl-10-methoxy-1,2,3,4,4a,5-hexahydrobenzo[b]pyrazino[1,2-d][1,4]diazepin-6(7h)-one

HRID 80495
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 80495
[NH2:1][C:2]1[CH:7]=[CH:6][C:5]([O:8][CH3:9])=[CH:4][C:3]=1[N:10]1[CH2:15][CH2:14]N(CC2C=CC=CC=2)[CH2:12][CH:11]1[CH2:23][C:24]([OH:26])=O.[N:27]1[CH:32]=[CH:31][CH:30]=[CH:29][CH:28]=1.Cl.CN(C)[CH2:36][CH2:37]CN=C=NCC>CN(C)C=O>[CH2:32]([N:27]1[CH2:14][CH2:15][N:10]2[C:3]3[CH:4]=[C:5]([O:8][CH3:9])[CH:6]=[CH:7][C:2]=3[NH:1][C:24](=[O:26])[CH2:23][CH:11]2[CH2:12]1)[C:31]1[CH:37]=[CH:36][CH:28]=[CH:29][CH:30]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 3

HCID 1049PyridineHCID 27239391,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 667697652-(1-(2-Amino-5-methoxyphenyl)-4-benzylpiperazin-2-yl)acetic acid

Produkt 1

HCID 667698133-Benzyl-10-methoxy-1,2,3,4,4a,5-hexahydrobenzo[b]pyrazino[1,2-d][1,4]diazepin-6(7h)-one

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6228
Dimethylformamide
Lösungsmittel

Versuchsvorschrift

To a solution of Example 12E (0.390 g, 1.097 mmol) in N,N-dimethylformamide (3.66 mL) were added pyridine (4.44 mL, 54.9 mmol) and N-(3-dimethylaminopropyl)-N′-ethylcarbodiimide hydrochloride (0.421 g, 2.195 mmol) and the mixture was stirred at room temperature for 1 hour. The solution was concentrated, water was added to the residue, and the product was extracted twice with ethyl acetate. The combined organic washes were dried over sodium sulfate, concentrated and dried under vacuum at room temperature overnight. It was then passed through a 5 gram silica gel cartridge eluting first with dichloromethane, then with 2% methanol/dichloromethane and finally with 5% methanol/dichloromethane to obtain the title compound. An aliquot of material was further purified for analytical purposes by preparative HPLC to afford the title compound as the trifluoroacetic acid salt. 1H NMR (500 MHz, DMSO-d6) δ ppm 10.21 (s, 1H), 9.52 (s, 1H), 7.54-7.48 (m, 5H), 6.90 (d, J=8.6, 1H), 6.70-6.60 (m, 2H), 4.45 (s, 2H), 3.74 (s, 3H), 3.67-3.07 (m, 7H), 3.22-3.04 (m, 2H), 2.61 (dd, J=7.0, 13.5, 1H), 2.00 (d, J=13.5, 1H); MS (ESI) m/z 338.1 (M+H)+.

Aufarbeitung

  1. concentrationThe solution was concentrated
  2. additionwater was added to the residue
  3. extractionthe product was extracted twice with ethyl acetate
  4. dry with materialThe combined organic washes were dried over sodium sulfate
  5. concentrationconcentrated
  6. customdried under vacuum at room temperature overnight
  7. washeluting first with dichloromethane

Quellen und Nachweise

ORD-Eintrag
ord-655a3e0a02bc4f9fa2fccaae604369b1
Quelldatensatz
uspto-grants-2014_09
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08846663B2

Notizen zur Reaktion

Wird geladen…

Auf dieser SeiteKomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion