Triethylamine → HCID 178501468、化合物
反応式
[OH:1][C:2]1[N:6]([C:7]2[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=2)[N:5]=[C:4]([C:13]([OH:15])=O)[CH:3]=1.Cl.[CH3:17][O:18][C:19](=[O:31])[C@@H:20]([NH2:30])[CH2:21][CH2:22][C:23]([O:25][C:26]([CH3:29])([CH3:28])[CH3:27])=[O:24].C(N(CC)CC)C.CN(C(ON1N=NC2C=CC=NC1=2)=[N+](C)C)C.F[P-](F)(F)(F)(F)F>C(Cl)Cl.O>[CH3:17][O:18][C:19](=[O:31])[C@@H:20]([NH:30][C:13]([C:4]1[CH:3]=[C:2]([OH:1])[N:6]([C:7]2[CH:8]=[CH:9][CH:10]=[CH:11][CH:12]=2)[N:5]=1)=[O:15])[CH2:21][CH2:22][C:23]([O:25][C:26]([CH3:27])([CH3:28])[CH3:29])=[O:24]参加物
7
反応物 4
生成物 1
試薬・触媒・溶媒 2
実験手順
To a solution of 8 g of 5-Hydroxy-1-phenyl-1H-pyrazole-3-carboxylic acid and 10 g of (S)-2-Amino-pentanedioic acid 5-tert-butyl ester 1-methyl ester hydrochloride in 300 ml of DCM, 16 g of triethylamine and 15 g of HATU was added and stirred for 16 h at RT. Then, the reaction mixture was diluted with water and extracted with DCM. The organic phase was dried over MgSO4 and the solvents were removed under reduced pressure. The crude product was purified by chromatography on silica gel eluting with a gradient of n-heptane/ethyl acetate. The fractions containing the product were combined and the solvent evaporated under reduced pressure. Yield: 11 g.
後処理
- extractionextracted with DCM
- dry with materialThe organic phase was dried over MgSO4
- customthe solvents were removed under reduced pressure
- customThe crude product was purified by chromatography on silica gel eluting with a gradient of n-heptane/ethyl acetate
- additionThe fractions containing the product
- customthe solvent evaporated under reduced pressure
出典と根拠
- ORDレコード
- ord-fd508d3428f849969432f12f9917ffca
- 出典データセット
- uspto-grants-2013_12
- 特許番号
- US08598179B2
反応ノート
読み込み中…