Water → 2-(Methyloxycarbonyl)amino-4-isopropyl-7-methyl-6-thiocyanato-benzothiazole

HRID 23462Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 23462
[CH:1]([C:4]1[C:9]2[N:10]=[C:11]([NH2:13])[S:12][C:8]=2[C:7]([CH3:14])=[C:6]([S:15][C:16]#[N:17])[CH:5]=1)([CH3:3])[CH3:2].Cl[C:19]([O:21][CH3:22])=[O:20].O.CCOC(C)=O>C(Cl)Cl.N1C=CC=CC=1>[CH3:22][O:21][C:19]([NH:13][C:11]1[S:12][C:8]2[C:7]([CH3:14])=[C:6]([S:15][C:16]#[N:17])[CH:5]=[C:4]([CH:1]([CH3:3])[CH3:2])[C:9]=2[N:10]=1)=[O:20]

Komponenten

7

Edukt 4

HCID 962WaterHCID 6586Methyl chloroformateHCID 8857Ethyl AcetateHCID 225729724-Isopropyl-7-methyl-6-thiocyanato-benzothiazol-2-yl-amine

Produkt 1

HCID 225730782-(Methyloxycarbonyl)amino-4-isopropyl-7-methyl-6-thiocyanato-benzothiazole

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 1049PyridineLösungsmittelHCID 6344DichloromethaneLösungsmittel

Versuchsvorschrift

To 4-isopropyl-7-methyl-6-thiocyanato-benzothiazol-2-yl-amine (Example L-4; 4.0 g, 17 mmol) dissolved in CH2Cl2 (25 mL) and pyridine (5 mL), was added methyl chloroformate at 0° C. The reaction mixture was stirred at room temperature for 2 hours. H2O was added to the reaction mixture followed by EtOAc (100 mL). The organic layer was washed with 2N HCl, H2O, saturated sodium bicarbonate solution and brine, and was dried (MgSO4). The solvents were evaporated, and the residue was purified by flash chromatography (100% hexanes to 25% EtOAc in hexanes) to give 2-(methyloxycarbonyl)amino-4-isopropyl-7-methyl-6-thiocyanato-benzothiazole. MS (APCI): 322 (M+H).

Aufarbeitung

  1. washThe organic layer was washed with 2N HCl, H2O, saturated sodium bicarbonate solution and brine
  2. dry with materialwas dried (MgSO4)
  3. customThe solvents were evaporated
  4. customthe residue was purified by flash chromatography (100% hexanes to 25% EtOAc in hexanes)

Quellen und Nachweise

ORD-Eintrag
ord-6a1054619fbc4fcb904c96e147584521
Quelldatensatz
uspto-grants-2005_02
Patentnummer
US06852711B2

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