Methyl chloroformate → HCID 10706453, Verbindung

HRID 1637381Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1637381
[CH3:1][S:2]([N:5]([CH3:11])[NH:6][S:7]([CH3:10])(=[O:9])=[O:8])(=[O:4])=[O:3].C(=O)([O-])[O-].[Na+].[Na+].Cl[C:19]([O:21][CH3:22])=[O:20]>CC(C)=O>[CH3:1][S:2]([N:5]([CH3:11])[N:6]([S:7]([CH3:10])(=[O:8])=[O:9])[C:19]([O:21][CH3:22])=[O:20])(=[O:3])=[O:4]

Komponenten

5

Versuchsvorschrift

1,2-Bis(methylsulfonyl)-2-(methoxycarbonyl)-1-methylhydrazine (compound 6) was synthesized as follows: A mixture of 1,2-bis(methylsulfonyl)-1-methylhydrazine (Shyam et al., J. Med. Chem. 30 2157-2161 (1987)) (1.00 g, 0.005 mol), anhydrous sodium carbonate (1.9 g, 0.018 mol), methyl chloroformate (1.23 g, 0.013 mol) and acetone (30 ml) was heated under reflux for 18 hr. The reaction mixture was filtered and the filtrate evaporated to dryness in vacuo. The residue, a thick oil, was stirred with methanol (5 ml) and cooled in ice. The solid that separated was filtered and recrystallized from ethanol-petroleum ether (0.63 g, 48.9%). The melting point (Mp) of this compound was found to be approximately 88-89° C. Analysis of the compound by 1H NMR (CDCl3) showed the following results: δ 0 4.0(3H, s, OCH3), 3.5, 3.4, 3.1 (9H, 3s, 2 CH3SO2 and NCH3).

Aufarbeitung

  1. temperaturewas heated
  2. temperatureunder reflux for 18 hr
  3. filtrationThe reaction mixture was filtered
  4. customthe filtrate evaporated to dryness in vacuo
  5. temperaturecooled in ice
  6. customThe solid that separated
  7. filtrationwas filtered
  8. customrecrystallized from ethanol-petroleum ether (0.63 g, 48.9%)
  9. customto be approximately 88-89° C
  10. customfollowing results

Quellen und Nachweise

ORD-Eintrag
ord-2a86cc42704c48a1b421e569ac21d672
Quelldatensatz
uspto-grants-2000_03
Patentnummer
US06040338

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