Реакция #69164

Уравнение реакции

2-methyl-2-[4-(1H-pyrrolo[2,3-b]pyridin-4-yl)-1H-pyrazol-1-yl]propanoic acid

N,N-carbonyldiimidazole

NH4Cl

→

2-methyl-2-[4-(1H-pyrrolo[2,3-b]pyridin-4-yl)-1H-pyrazol-1-yl]propanamide

Выход 26.2%

Растворители

DMF

Условия реакции

Обработка

1. 1
   workup.STIRRINGthis was stirred for 3 hours
2. 2
   ДругоеThe majority of solvent was removed in vacuo
3. 3
   Другоеthe crude residue was purified by preparative-HPLC (
4. 4
   ПромывкаC18 eluting with a gradient of ACN/H2O containing 0.1% TFA)
5. 5
   Другоеfollowed by re-purification via preparative-HPLC (
6. 6
   ПромывкаC18 eluting with a gradient of ACN/H2O containing 0.15% NH4OH)

Методика

A mixture of 2-methyl-2-[4-(1H-pyrrolo[2,3-b]pyridin-4-yl)-1H-pyrazol-1-yl]propanoic acid (23 mg, 0.000085 mol) and N,N-carbonyldiimidazole (CDI) (21 mg, 0.00013 mol) in 2 mL of DMF was stirred for 3 hours. An excess of solid NH4Cl and TEA was added to the mixture and this was stirred for 3 hours. The majority of solvent was removed in vacuo, and the crude residue was purified by preparative-HPLC (C18 eluting with a gradient of ACN/H2O containing 0.1% TFA) followed by re-purification via preparative-HPLC (C18 eluting with a gradient of ACN/H2O containing 0.15% NH4OH) to afford 2-methyl-2-[4-(1H-pyrrolo[2,3-b]pyridin-4-yl)-1H-pyrazol-1-yl]propanamide (6 mg, 26%). 1H NMR (400 MHz, d6-DMSO): δ □11.63 (s, 1H), 8.44 (s, 1H), 8.16 (s, 1H), 8.14 (s, 1H), 7.47 (t, 1H), 7.29 (d, 1H), 7.21 (s, 1H), 6.93 (s, 1H), 6.80 (dd, 1H), 1.77 (s, 6H); MS (ES): 270 (M+1).

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