Triethylamine → 6-chloro-1H-imidazo[4,5-c]pyridine-2(3H)-thione

HRID 929182

Reaktionsgleichung

Reaktionsgleichung von HRID 929182
[Cl:1][C:2]1[N:7]=[CH:6][C:5]([NH2:8])=[C:4]([NH2:9])[CH:3]=1.[C:10](N1C=CN=C1)(N1C=CN=C1)=[S:11].C(N(CC)CC)C>CN(C=O)C>[Cl:1][C:2]1[N:7]=[CH:6][C:5]2[NH:8][C:10](=[S:11])[NH:9][C:4]=2[CH:3]=1

Komponenten

5

Versuchsvorschrift

A stirred mixture of 6-chloropyridine-3,4-diamine (500 mg, 3.48 mmol), 1,1′-thiocarbonyldiimidazole (1.24 g, 6.97 mmol), and triethylamine (0.49 mL, 3.48 mmol) in anhydrous DMF (15.0 mL) was microwaved in a Biotage Initiator at 100° C. at normal power for 1 h. Then the reaction mixture was evaporated at reduced pressure, and the resulting residue extracted with DCM (200 mL) and allowed to stand at 10° C. overnight. The mixture filtered and the solids washed with cold DCM (2×20 mL), and air dried to afford the title compound as a solid. LC-MS: calculated for C6H4ClN3S 184.98 observed m/e: 186.07 (M+H)+ (Rt 0.62/2.0 min)

Aufarbeitung

  1. customwas microwaved in a Biotage Initiator at 100° C. at normal power for 1 h
  2. customThen the reaction mixture was evaporated at reduced pressure
  3. extractionthe resulting residue extracted with DCM (200 mL)
  4. filtrationThe mixture filtered
  5. washthe solids washed with cold DCM (2×20 mL), and air
  6. customdried

Quellen und Nachweise

ORD-Eintrag
ord-dfb30f55ec3e46d28a7030b19bf08bed
Quelldatensatz
uspto-grants-2016_03
Patentnummer
US09290517B2

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