참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Hydrochloric Acid | HCID 313 | — |
| 반응물 | Methanol | HCID 887 | — |
| 반응물 | Lithium Hydroxide | HCID 3939 | — |
| 반응물 | 2-(4-methoxybenzylthio)-pentanoyl-(L)-homophenylalanine methyl ester | HCID 22950828 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 용매 | Ethyl acetate hexane | HCID 21226206 | — |
| 생성물 | 2-(4-methoxybenzylthio)-pentanoyl-(L)-homophenylalanine | HCID 22950827 | — |
반응 단계
Combine 2-(4-methoxybenzylthio)-pentanoyl-(L)-homophenylalanine methyl ester (3.50 g, 8.15 mmol) and methanol (30 mL)and tetrahydrofuran (30 (mL). Cool in an ice bath. Add an aqueous 2M lithium hydroxide solution (8.2 mL, 16.4 mmol). After 18 hours, adjust the pH to about 6 using an aqueous 10% hydrochloric acid solution and evaporate in vacuo to give a residue. Partition the residue between dichloromethane and water, adjust the pH of the aqueous layer to about 1 using an aqueous 10% hydrochloric acid solution. Separate the layers, extract the aqueous layer repeatedly with ethyl acetate. Combine the organic layers, dry over Na2SO4, filter, and evaporate in vacuo to give a residue. Chromatograph the residue on silica gel eluting with 95% 1/1 hexane/ethyl acetate/5% acetic acid to give the title compound.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06352976B1 |
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| 출처 데이터셋 | uspto-grants-2002_03 |
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| ORD ID | ord-222d2ac6f50248dabfb0e58127fe60d6 |
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| 출처 메모 | uspto-grants-2002_03 |
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