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1,2-Dichloroethane → N-(2-((2-(Methoxymethyl)oxazol-4-yl)methyl)-2H-1,2,3-triazol-4-yl)-2-methyl-5-(m-tolyl)oxazole-4-carboxamide

HRID 82799
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Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 82799
N#N.[CH3:3][C:4]1[O:5][C:6]([C:12]2[CH:13]=[C:14]([CH3:18])[CH:15]=[CH:16][CH:17]=2)=[C:7]([C:9]([OH:11])=O)[N:8]=1.C1C=CC2N(O)N=NC=2C=1.C(Cl)CCl.CCN(C(C)C)C(C)C.[CH3:42][O:43][CH2:44][C:45]1[O:46][CH:47]=[C:48]([CH2:50][N:51]2[N:55]=[C:54]([NH2:56])[CH:53]=[N:52]2)[N:49]=1>C(Cl)Cl.CN(C1C=CN=CC=1)C>[CH3:42][O:43][CH2:44][C:45]1[O:46][CH:47]=[C:48]([CH2:50][N:51]2[N:55]=[C:54]([NH:56][C:9]([C:7]3[N:8]=[C:4]([CH3:3])[O:5][C:6]=3[C:12]3[CH:13]=[C:14]([CH3:18])[CH:15]=[CH:16][CH:17]=3)=[O:11])[CH:53]=[N:52]2)[N:49]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

9

Edukt 6

HCID 111,2-DichloroethaneHCID 947NitrogenHCID 757711-HydroxybenzotriazoleHCID 81531DiisopropylethylamineHCID 669292052-Methyl-5-(m-tolyl)oxazole-4-carboxylic acidHCID 679583082-((2-(methoxymethyl)oxazol-4-yl)methyl)-2H-1,2,3-triazol-4-amine

Produkt 1

HCID 67968164
N-(2-((2-(Methoxymethyl)oxazol-4-yl)methyl)-2H-1,2,3-triazol-4-yl)-2-methyl-5-(m-tolyl)oxazole-4-carboxamide

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 142844-(Dimethylamino)pyridineKatalysatorHCID 6344DichloromethaneLösungsmittel3×

Versuchsvorschrift

In a flame dried round-bottomed flask equipped with a magnetic stir bar and under inert atmosphere (N2), a solution of 2-methyl-5-(m-tolyl)oxazole-4-carboxylic acid (WO 2009/077990, p. 112) (14 mg, 0.06 mmol) in CH2Cl2 (0.3 mL) was treated at rt with DMAP (2 mg, 0.02 mmol), HOBt (10 mg, 0.08 mmol), EDC (31 mg, 0.16 mmol) and DIPEA (0.04 mL, 0.26 mmol) and the resulting mixture was stirred for 45 min at rt. A solution of 2-((2-(methoxymethyl)oxazol-4-yl)methyl)-2H-1,2,3-triazol-4-amine (13 mg, 0.06 mmol) in CH2Cl2 (0.3 mL) was then added and the reaction mixture was stirred overnight at rt. The mixture was diluted with CH2Cl2 (5 mL), the org. phase was washed with water (5 mL), dried over Na2SO4, filtered and the solvents were removed under reduced pressure. Purification of the residue by FC (1:2 hept-EA) gave the title compound as a colorless oil: TLC: rf (1:2 hept-EA)=0.36. LC-MS-conditions 07: tR=0.88 min, [M+H]+=408.69.

Aufarbeitung

  1. stirringthe reaction mixture was stirred overnight at rt
  2. washphase was washed with water (5 mL)
  3. dry with materialdried over Na2SO4
  4. filtrationfiltered
  5. customthe solvents were removed under reduced pressure
  6. customPurification of the residue by FC (1:2 hept-EA)

Quellen und Nachweise

ORD-Eintrag
ord-1c9f2a74133d4409bf61bc55c848a493
Quelldatensatz
uspto-grants-2014_09
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08846733B2

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