Triethylamine → HCID 86665067、化合物
反応式
[CH2:1]([O:8][C:9](=[O:19])[CH2:10][C:11]1([C:16]([OH:18])=O)[CH2:15][CH2:14][CH2:13][CH2:12]1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[NH2:20][C@@H:21]([C:35]1[N:39]([CH2:40][CH2:41][C:42]#[N:43])[N:38]=[N:37][N:36]=1)[CH2:22][C:23]1[CH:28]=[CH:27][C:26]([C:29]2[CH:34]=[CH:33][CH:32]=[CH:31][CH:30]=2)=[CH:25][CH:24]=1.CCN=C=NCCCN(C)C.Cl.C1C=NC2N(O)N=NC=2C=1.C(N(CC)CC)C>CN(C=O)C.CCOC(C)=O>[C:26]1([C:29]2[CH:30]=[CH:31][CH:32]=[CH:33][CH:34]=2)[CH:25]=[CH:24][C:23]([CH2:22][C@@H:21]([NH:20][C:16]([C:11]2([CH2:10][C:9]([O:8][CH2:1][C:2]3[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=3)=[O:19])[CH2:12][CH2:13][CH2:14][CH2:15]2)=[O:18])[C:35]2[N:39]([CH2:40][CH2:41][C:42]#[N:43])[N:38]=[N:37][N:36]=2)=[CH:28][CH:27]=1参加物
反応物 5
生成物 1
試薬・触媒・溶媒 2
実験手順
To a solution of 1-(2-(benzyloxy)-2-oxoethyl)cyclopentanecarboxylic acid (49.4 mg, 0.188 mmol) and (R)-3-(5-(1-amino-2-(biphenyl-4-yl)ethyl)-1H-tetrazol-1-yl)propanenitrile (50 mg, 0.157 mmol) in DMF (1.5 mL) were added EDC.HCl (36 mg, 0.188 mmol), HOAt (26 mg, 0.188 mmol) and triethylamine (0.033 mL, 0.236 mmol). After being stirred for 2 hours, the reaction mixture was diluted with EtOAc. The mixture was washed with H2O2O and brine, dried over Na2SO4 and concentrated. The residue was purified by silica gel flash column chromatography (eluent; EtOAc/heptane) to give (R)-benzyl 2-(1-(2-(biphenyl-4-yl)-1-(1-(2-cyanoethyl)-1H-tetrazol-5-yl)ethylcarbamoyl)cyclopentyl)acetate (39 mg). LCMS (condition A) δ 563 (M+1); retention time=1.85 min.
後処理
- washThe mixture was washed with H2O2O and brine
- dry with materialdried over Na2SO4
- concentrationconcentrated
- customThe residue was purified by silica gel flash column chromatography (eluent; EtOAc/heptane)
出典と根拠
- ORDレコード
- ord-7894521324934f12a7a1d66cd91e2fc1
- 出典データセット
- uspto-grants-2014_11
- 特許番号
- US08877815B2
反応ノート
読み込み中…