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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
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Diisopropylcarbodiimide | HCID 12734 | — |
| 反応物 | 1-Hydroxybenzotriazole | HCID 75771 | — |
| 反応物 | 2-([1,1'-Biphenyl]-2-yl)ethanamine | HCID 21921242 | — |
| 反応物 | 3-Carboxy-2-phenethyl-pentandioic acid 5-tert-butyl ester 1-methyl ester | HCID 69212314 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | 3-(2-Biphenyl-4-yl-ethylcarbamoyl)-2-phenethyl-pentanedioic acid 5-tertbutyl ester 1-methyl ester | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07365091B2 |
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| 出典データセット | uspto-grants-2008_04 |
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| ORD ID | ord-7b2295d010ff4a6dae3bc37439442802 |
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| 出典メモ | uspto-grants-2008_04 |
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