Reaktion #675366

Reaktionsgleichung

6-Chloro-3-methoxy-1H-pyrazolo[4,3-c]pyridine

1-((3S,4R)-1-methyl-4-phenylpyrrolidin-3-yl)urea

Intermediate 17B

1-((3S,4R)-1-methyl-4-phenylpyrrolidin-3-yl)urea

potassium tert-butoxide

→

1-(3-methoxy-1H-pyrazolo[4,3-c]pyridin-6-yl)-3-[(3S,4R)-1-methyl-4-phenylpyrrolidin-3-yl]urea

Lösungsmittel

THF

Reaktionsbedingungen

Aufarbeitung

1. 1
   SonstigeThe vial was degassed with argon for 5 min
2. 2
   FiltrationThe reaction mixture was filtered through Celite
3. 3
   Wascheneluting with MeOH
4. 4
   Einengenthe filtrate was concentrated in vacuo
5. 5
   SonstigePurification by flash chromatography (0-20% CH2Cl2/MeOH with 1% ammonia)

Vorschrift

6-Chloro-3-methoxy-1H-pyrazolo[4,3-c]pyridine (50 mg, 0.272 mmol), 1-((3S,4R)-1-methyl-4-phenylpyrrolidin-3-yl)urea (Intermediate 17B; 90 mg, 0.409 mmol), BrettPhos pre-catalyst (21.75 mg, 0.027 mmol), and potassium tert-butoxide (1 M in THF, 0.817 mL, 0.817 mmol) were dissolved in THF (1 mL). The vial was degassed with argon for 5 min and the reaction stirred at 60° C. for 16 h. The reaction mixture was filtered through Celite, eluting with MeOH, and the filtrate was concentrated in vacuo while loading onto silica gel. Purification by flash chromatography (0-20% CH2Cl2/MeOH with 1% ammonia) gave 1-(3-methoxy-1H-pyrazolo[4,3-c]pyridin-6-yl)-3-[(3S,4R)-1-methyl-4-phenylpyrrolidin-3-yl]urea. MS ESI calc'd. For C19H22N6O2 [M+1]+ 367. found 367. 1H NMR (500 MHz, DMSO-d6) δ 11.97 (s, 1H), 8.89 (s, 1H), 8.51 (s, 1H), 7.72 (s, 1H), 7.43 (s, 1H), 7.31-7.26 (m, 3H), 7.22-7.18 (m, 2H), 4.22-4.14 (m, 1H), 3.98 (s, 3H), 3.16-3.04 (m, 1H), 2.64-2.58 (m, 2H), 2.48 (s, 3H), 2.38-2.28 (m, 2H).

Quelle