反応式
[CH:1](N(CC)C(C)C)([CH3:3])[CH3:2].[CH3:10][C:11]1[CH:16]=[CH:15][C:14]([C:17]2([C:20]([OH:22])=O)[CH2:19][CH2:18]2)=[CH:13][CH:12]=1.CN(C([O:30][N:31]1N=NC2C=CC=NC1=2)=[N+](C)C)C.F[P-](F)(F)(F)(F)F.C([O:50][CH2:51][CH3:52])(=O)C.C[N:54](C)C=O>>[OH:30][NH:31][C:51]([C@H:52]([NH:54][C:20]([C:17]1([C:14]2[CH:13]=[CH:12][C:11]([CH3:10])=[CH:16][CH:15]=2)[CH2:18][CH2:19]1)=[O:22])[CH:1]([CH3:3])[CH3:2])=[O:50]参加物
6
反応物 5
生成物 1
反応条件
- 温度
- 70 °C
実験手順
N,N-diisopropylethylamine (0.539 mL, 4 eq) was added to a mixture of the crude amine hydrochloride (200 mg) from reaction (1b), 1-(4-methylphenyl)-1-cyclopropane carboxylic acid (163 mg, 1.2 eq) and HATU (441 mg, 1.5 eq) in N,N-dimethylformamide (1 mL). The mixture was stirred at room temperature overnight and at 70° C. for 90 min. Following addition of ethyl acetate (100 mL), the mixture was washed with 1:1 mixture of 1 N hydrochloric acid-saturated brine (2×10 mL), dried (MgSO4) and concentrated. Silica gel column chromatography (ethyl acetate-hexane, 40:60) yielded the desired product (127 mg, 52% for two steps). MS found: (M+H)+=381.
後処理
- washthe mixture was washed with 1:1 mixture of 1 N hydrochloric acid-saturated brine (2×10 mL)
- dry with materialdried (MgSO4)
- concentrationconcentrated
出典と根拠
- ORDレコード
- ord-120696545c394922ba8455a52aa0effd
- 出典データセット
- uspto-grants-2002_04
- 特許番号
- US06376665B1
関連ノート
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