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HRID 902922作成日:2026年10月27日

Diisopropylcarbodiimide → 3-(2-Biphenyl-4-yl-ethylcarbamoyl)-2-phenethyl-pentanedioic acid 5-tertbutyl ester 1-methyl ester

https://huagongshe.com/reaction/902922

反応式

関与物質

役割名称HCID仕込み量
反応物DiisopropylcarbodiimideHCID 12734—
反応物1-HydroxybenzotriazoleHCID 75771—
反応物2-([1,1'-Biphenyl]-2-yl)ethanamineHCID 21921242—
反応物3-Carboxy-2-phenethyl-pentandioic acid 5-tert-butyl ester 1-methyl esterHCID 69212314—
溶媒DimethylformamideHCID 6228—
生成物3-(2-Biphenyl-4-yl-ethylcarbamoyl)-2-phenethyl-pentanedioic acid 5-tertbutyl ester 1-methyl esterHCID 69209468—

反応手順

A solution of the compound of example 53 (590 mg, 1.68 mmol) and HOBt (272 mg, 2.016 mmol) in anhydrous DMF was stirred in an ice bath for 10 minutes. Biphenyl ethylamine (404 mg, 2.02 mmol) was added followed by the addition of DIC (320 μL, 2.01 mmol). After 20 minutes, the ice bath was removed and stirring was continued at room temperature. After 24 h of stirring, the reaction mixture was partitioned between ethyl acetate and HCl (1M, excess). The aqueous phase was extracted several times with ethyl acetate. The recombined organic layer was extracted with brine, saturated sodium hydrogen carbonate, and brine. The solvent was evaporated following drying over sodium sulfate and filtration. The crude was flashed using 25% EtOAc in hexanes. 1H-NMR(CDCl3, 300 MHz: 1.41(s, 9H); 1.82(m, 2H); 2.23(m, 1H); 2.55(t, J=8.1 Hz, 2H); 2.75(m, 5H); 3.54(m, 1H); 3.70(s, 3H); 6.09(t, J=5.7 Hz, 1H); 7.13-7.36, 7.41-7.49, 7.55-7.58(m, 14H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07365091B2
出典データセットuspto-grants-2008_04
ORD IDord-7b2295d010ff4a6dae3bc37439442802
出典メモuspto-grants-2008_04