反应详情
EQUATION
反应方程式
REACTANTS
反应物
PRODUCTS
生成物
AUXILIARIES
试剂、催化剂与溶剂
PROCEDURE
实验过程
A solution of (R)-2-(2-(2,4-dimethoxybenzyl)-7-fluoro-4-(1-methyl-1H-pyrazol-4-yl)-3-oxo-2,3-dihydro-1H-pyrrolo[3,4-c]pyridin-6-ylamino)-4-methylpentanamide (39.8 mg, 0.078 mmol) in TFA (5 mL) was heated at 60° C. for 2 h. After removal of solvent, the residue was diluted in MeOH (2 mL) and was purified by preparative HPLC. The fractions were collected and the solvent stripped to dryness via rotary evaporation to yield the title compound (12.8 mg, 46%). 1H NMR (500 MHz, DMSO-d6) δ ppm 0.82-1.00 (m, 6 H), 1.45-1.60 (m, 1 H), 1.67-1.83 (m, 2 H), 3.87 (s, 3 H), 4.36 (s, 2 H), 4.50-4.64 (m, 1 H), 6.88-7.02 (m, 2 H), 7.44 (s, 1 H), 8.28 (s, 2 H), 8.83 (s, 1 H). [M+H] calc'd for C17H21FN6O2, 361; found, 361.
WORKUP
后处理
- customAfter removal of solvent
- additionthe residue was diluted in MeOH (2 mL)
- customwas purified by preparative HPLC
- customThe fractions were collected
- customthe solvent stripped to dryness via rotary evaporation