Trityl chloride → Phenyl [1-methyl-5-(tritylamino)pyrazol-4-yl]carbamate

HRID 459607Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 459607
[NH2:1][C:2]1[N:6]([CH3:7])[N:5]=[CH:4][C:3]=1[NH:8][C:9]([O:11][C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1)=[O:10].C(N(CC)CC)C.[C:25]1([C:31](Cl)([C:38]2[CH:43]=[CH:42][CH:41]=[CH:40][CH:39]=2)[C:32]2[CH:37]=[CH:36][CH:35]=[CH:34][CH:33]=2)[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=1.CCCCCCC>O1CCCC1>[CH3:7][N:6]1[C:2]([NH:1][C:31]([C:25]2[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=2)([C:38]2[CH:39]=[CH:40][CH:41]=[CH:42][CH:43]=2)[C:32]2[CH:33]=[CH:34][CH:35]=[CH:36][CH:37]=2)=[C:3]([NH:8][C:9]([O:11][C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=2)=[O:10])[CH:4]=[N:5]1

Komponenten

6

Edukt 4

HCID 6456Trityl chlorideHCID 8471TriethylamineHCID 8900HeptaneHCID 219044605-Amino-1-methyl-4-phenoxycarbonylaminopyrazole

Produkt 1

HCID 21904567Phenyl [1-methyl-5-(tritylamino)pyrazol-4-yl]carbamateAusbeute 80,7 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8028TetrahydrofuranLösungsmittel

Versuchsvorschrift

To a suspension of 5-amino-1-methyl-4-phenoxycarbonylaminopyrazole (153.8 g) in tetrahydrofuran (1 L) were added triethylamine (67 g) and triphenylmethyl chloride (185 g) at room temperature. The mixture was stirred for 6.5 hours. To the reaction mixture was added heptane (2.6 L) and the mixture was stirred for 1 hour. The precipitated solid was collected by filtration and washed with heptane-diisopropyl ether (1:1). The crude solid was suspended in water (3 L) and the suspension was stirred for 1 hour. The solid was collected by filtration and dried to give 1-methyl-4-phenoxycarbonylamino-5-triphenylmethylaminopyrazole (253.6 g).

Aufarbeitung

  1. stirringthe mixture was stirred for 1 hour
  2. filtrationThe precipitated solid was collected by filtration
  3. washwashed with heptane-diisopropyl ether (1:1)
  4. stirringthe suspension was stirred for 1 hour
  5. filtrationThe solid was collected by filtration
  6. customdried

Quellen und Nachweise

ORD-Eintrag
ord-357565b0423249bda79dfe4b191372f4
Quelldatensatz
uspto-grants-2007_03
Patentnummer
US07192943B2

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