反応 #1509576
ord-8856ebaee96b4a24a0e75bfb0b96c6a7
反応方程式
1-[1-(4-Chloro-3-methyl-benzyl)-piperidin-4-yl]-5-oxo-pyrrolidine-2-carboxylic acid
DIPEA
DIPEA
HATU
3-Bromo-5-(1-methyl-1H-tetrazol-5-yl)-phenylamine
→
title compound
1-[1-(4-Chloro-3-methyl-benzyl)-piperidin-4-yl]-5-oxo-pyrrolidine-2-carboxylic acid [3-bromo-5-(1-methyl-1H-tetrazol-5-yl)-phenyl]-amide
反応物
試薬
なし
溶媒
反応条件
詳細条件
See reaction.notes.procedure_details.
後処理
- 1ろ過The reaction mixture was filtered
- 2その他the filtrate partitioned between water and EtOAc
- 3その他The organic layer was separated
- 4その他dried
- 5濃縮concentrated in vacuum
- 6その他the residue purified by flash chromatography (DCM:MeOH 100:0 to 95:5 gradient)
実験手順
To a solution of 1-[1-(4-Chloro-3-methyl-benzyl)-piperidin-4-yl]-5-oxo-pyrrolidine-2-carboxylic acid as DIPEA salt (2.6 g) in DMF (100 ml) was added DIPEA (2.1 g), and HATU (4 g). 3-Bromo-5-(1-methyl-1H-tetrazol-5-yl)-phenylamine (1.4 g) was added and the reaction stirred overnight at rt. The reaction mixture was filtered and the filtrate partitioned between water and EtOAc. The organic layer was separated, dried and concentrated in vacuum and the residue purified by flash chromatography (DCM:MeOH 100:0 to 95:5 gradient) to give the title compound (400 mg). Rf=0.19 (95:5 DCM:MeOH).