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3,4-Dichlorobenzoic acid → Methyl (5-{4-[(3,4-dichloro-benzoyl)amino]benzyl}imidazo[1,2-c]pyrimidin-8-yl)acetate

HRID 2353325
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Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 2353325
[N+:1]([C:4]1[CH:24]=[CH:23][C:7]([CH2:8][C:9]2[N:14]3[CH:15]=[CH:16][N:17]=[C:13]3[C:12]([CH2:18][C:19]([O:21][CH3:22])=[O:20])=[CH:11][N:10]=2)=[CH:6][CH:5]=1)([O-])=O.NC1C=CC(CC2N3C=CN=C3C(CC(OC)=O)=CN=2)=CC=1.[Cl:47][C:48]1[CH:49]=[C:50]([CH:54]=[CH:55][C:56]=1[Cl:57])[C:51](O)=[O:52].ON1C2C=CC=CC=2N=N1.C(N(CC)CC)C.Cl.C(N=C=NCCCN(C)C)C>CO.C(OCC)(=O)C.[Pd].ClCCl>[Cl:47][C:48]1[CH:49]=[C:50]([CH:54]=[CH:55][C:56]=1[Cl:57])[C:51]([NH:1][C:4]1[CH:24]=[CH:23][C:7]([CH2:8][C:9]2[N:14]3[CH:15]=[CH:16][N:17]=[C:13]3[C:12]([CH2:18][C:19]([O:21][CH3:22])=[O:20])=[CH:11][N:10]=2)=[CH:6][CH:5]=1)=[O:52]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

11

Edukt 6

HCID 58173,4-Dichlorobenzoic acidHCID 8471TriethylamineHCID 757711-HydroxybenzotriazoleHCID 27239391,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 57542079Methyl [5-(4-aminobenzyl)imidazo[1,2-c]pyrimidin-8-yl]acetateHCID 57542081
Methyl [5-(4-nitrobenzyl)imidazo[1,2-c]pyrimidin-8-yl]acetate

Produkt 1

HCID 57542077Methyl (5-{4-[(3,4-dichloro-benzoyl)amino]benzyl}imidazo[1,2-c]pyrimidin-8-yl)acetateAusbeute 70 %

Reagenzien, Katalysatoren, Lösungsmittel 4

HCID 23938PalladiumKatalysatorHCID 887MethanolLösungsmittelHCID 6344DichloromethaneLösungsmittelHCID 8857Ethyl AcetateLösungsmittel

Versuchsvorschrift

A mixture of methyl [5-(4-nitrobenzyl)imidazo[1,2-c]pyrimidin-8-yl]acetate (28 mg, 0.09 mmol) and Pd/C (wet, 3 mg) in methanol (1 mL) was stirred under hydrogen atmosphere for 1 hour. After the removal of Pd/C by filtration through a Celite pad, the filtrate was concentrated in vacuo. The resulting crude methyl [5-(4-aminobenzyl)imidazo[1,2-c]pyrimidin-8-yl]acetate (26 mg, 0.09 mmol) was dissolved with dichloromethane (1 mL). To this solution was added 3,4-dichloro-benzoic acid (20.1 mg, 0.11 mmol), 1-hydroxybenzotriazole (14.2 mg, 0.11 mmol), triethylamine (0.037 mL, 0.26 mmol) and 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (21.9 mg, 0.11 mmol) at room temperature. The mixture was stirred at room temperature overnight, and diluted with ethyl acetate. The solution was washed with water and brine, dried over sodium sulfate, filtered and concentrated under reduced pressure. The crude product was purified by preparative TLC (silica gel, chloroform:methanol, 19:1) to give methyl (5-{4-[(3,4-dichloro-benzoyl)amino]benzyl}imidazo[1,2-c]pyrimidin-8-yl)acetate (29 mg, 70%) as slightly yellow oil.

Aufarbeitung

  1. customAfter the removal of Pd/C
  2. filtrationby filtration through a Celite pad
  3. concentrationthe filtrate was concentrated in vacuo
  4. stirringThe mixture was stirred at room temperature overnight
  5. washThe solution was washed with water and brine
  6. dry with materialdried over sodium sulfate
  7. filtrationfiltered
  8. concentrationconcentrated under reduced pressure
  9. customThe crude product was purified by preparative TLC (silica gel, chloroform:methanol, 19:1)

Quellen und Nachweise

ORD-Eintrag
ord-fe13bb9cf76b457181ff68c32f5c2051
Quelldatensatz
uspto-grants-2010_07
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07750014B2

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