反応 #1509576

ord-8856ebaee96b4a24a0e75bfb0b96c6a7

反応方程式

Cc1cc(CN2CCC(N3C(=O)CCC3C(=O)O)CC2)ccc1Cl
1-[1-(4-Chloro-3-methyl-benzyl)-piperidin-4-yl]-5-oxo-pyrrolidine-2-carboxylic acid
CCN(C(C)C)C(C)C
DIPEA
CCN(C(C)C)C(C)C
DIPEA
CN(C)C(On1nnc2cccnc21)=[N+](C)C.F[P-](F)(F)(F)(F)F
HATU
Cn1nnnc1-c1cc(N)cc(Br)c1
3-Bromo-5-(1-methyl-1H-tetrazol-5-yl)-phenylamine
Cc1cc(CN2CCC(N3C(=O)CCC3C(=O)Nc3cc(Br)cc(-c4nnnn4C)c3)CC2)ccc1Cl
title compound
Cc1cc(CN2CCC(N3C(=O)CCC3C(=O)Nc3cc(Br)cc(-c4nnnn4C)c3)CC2)ccc1Cl
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

溶媒

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    ろ過The reaction mixture was filtered
  2. 2
    その他the filtrate partitioned between water and EtOAc
  3. 3
    その他The organic layer was separated
  4. 4
    その他dried
  5. 5
    濃縮concentrated in vacuum
  6. 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).

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: USRE045323E1uspto-grants-2015_01