Pyridine → HCID 69558667, compound

Participants

Reaction Steps

To a solution of 150 mg (0.371 mmol) of [[2-(methylthio)-6-ethyl-7-[(3-chlorophenyl)methyl]-7H-pyrrolo[2,3-d]pyrimidin-4-yl]oxy]acetic acid methyl ester in 5 mL of chloroform was added 0.10 mL of oxalyl chloride followed by 0.04 mL of pyridine. The reaction stirred at ambient temperature and was monitored by nmr for conversion to product. Additional oxalyl chloride (0.030 mL) was added after 24 hours. After 48 hours, the reaction was quenched into 4.0 mL of dilute ammonium hydroxide and the product was extracted into 5.0 mL of methylene chloride. The organic phase was washed with water, dried with sodium sulfate and concentrated to 400 mg of yellow solid. The residue was purified by flash chromatography (38 g of silica, ethyl acetate) to provide 109 mg (62%) of [[2-(methylthio)-5-(aminooxoacetyl)-6-ethyl-7-[(3-chlorophenyl)methyl]-7H-pyrrolo[2,3-d]pyrimidin-4-yl]oxy]acetic acid methyl ester as a solid. nmr (300 MHz, dmso-d6) δ1.00 (t, 3H), 2.45 (s, 3H), 2.90 (q, 2H), 3.65 (s, 3H), 4.97 (s, 2H), 5.52 (s, 2H), 7.01 (m, 1H), 7.31 .(m, 3H), 7.60 (s, 1H), 8.02 (s, 1H)

Provenance & Evidence