Reaktion #306439

Reaktionsgleichung

1-(6-chloropyridazin-3-yl)hydrazine

2-(quinolin-6-yl)propanoic acid

DIEA

→

N′-(6-chloropyridazin-3-yl)-2-(quinolin-6-yl)propanehydrazide

Lösungsmittel

DMF

Reaktionsbedingungen

Aufarbeitung

1. 1
   workup.STIRRINGAfter 20 h stirring at 23° C.
2. 2
   Sonstigethe reaction was then partitioned between 9:1 CHCl3/IPA (100 mL) and 5% NaHCO3 (50 mL)
3. 3
   TrocknenThe organic phase was then dried over MgSO4
4. 4
   Einengenconcentrated to an oil
5. 5
   Sonstigepurified on silica (120 g)
6. 6
   Wascheneluting with 0>10% of 2 M NH3 in MeOH/DCM
7. 7
   SonstigeThe product was isolated as an off white solid

Vorschrift

To a stirring solution of 2-(quinolin-6-yl)propanoic acid (3260 mg, 16201 μmol) and DIEA (2830 μl, 16201 μmol) in DMF (25 mL) was added o-(7-azabenzotriazol-1-yl)-n,n,n′,n-tetramethyl uronium hexafluorophosphate (6160 mg, 16201 μmol) whole at 23° C. under nitrogen. The solution was stirred for 60 min, cooled to 0° C., then added 1-(6-chloropyridazin-3-yl)hydrazine (2342 mg, 16201 μmol). After 20 h stirring at 23° C., the reaction was then partitioned between 9:1 CHCl3/IPA (100 mL) and 5% NaHCO3 (50 mL). The organic phase was then dried over MgSO4, concentrated to an oil, then purified on silica (120 g) eluting with 0>10% of 2 M NH3 in MeOH/DCM. The product was isolated as an off white solid. MS (ESI pos. ion) m/z: 328 (MH+). Calc'd exact mass for C16H14ClN5O: 327.

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