Reaktion #1869352

ord-a0887a0e8931430f991311bcea63e31a

Reaktionsgleichung

O=S(=O)(O)O
sulfuric acid
Cc1nsc(N)c1C#N
5-amino-3-methylisothiazole-4-carbonitrile
N
ammonia
Cc1nsc(N)c1C(N)=O
5-Amino-3-methylisothiazole-4-carboxamide
Ausbeute 80.0%

Reaktionsbedingungen

Temperatur
70°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    TemperaturThe temperature was maintained below 55° C
  2. 2
    workup.ADDITIONwas charged to pH 10
  3. 3
    TemperaturThe mixture was cooled to 20° C., aged overnight
  4. 4
    Filtrationfiltered
  5. 5
    WaschenThe resulting solid was washed with dilute ammonia (3.6 volumes)
  6. 6
    Sonstigedried at 40° C.
  7. 7
    Sonstigeto give a pale brown solid (typical yield 80%)

Vorschrift

To a chilled solution of sulfuric acid (7.2 volumes, 12.9 equivs) was charged 5-amino-3-methylisothiazole-4-carbonitrile (method 4) (1.0 equiv). The temperature was maintained below 55° C. The reaction mixture was heated to 70° C. and held for 1 hour until TLC showed disappearance of starting material. The mixture was cooled to 60-65° C. before the ammonia (21 volumes) was charged to pH 10. The mixture was cooled to 20° C., aged overnight and filtered. The resulting solid was washed with dilute ammonia (3.6 volumes) and dried at 40° C. to give a pale brown solid (typical yield 80%).1H NMR (300 MHz, DMSO-d6) δ 2.46(s, 3H), 6.28 (s, 1H).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07498333B2uspto-grants-2009_03