참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | N,N-Dimethylaniline | HCID 949 | — |
| 반응물 | Ethyl Acetate | HCID 8857 | — |
| 반응물 | Benzyl chloroformate | HCID 10387 | — |
| 반응물 | Pyrrolidinone, (4-aminophenyl)- | HCID 676146 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | (5S)-5-(Aminomethyl)-3-[4-(2-oxo-1-pyrrolidinyl)phenyl]-1,3-oxazolidin-2-one | HCID 11666268 | — |
반응 단계
At −20° C., benzyl chloroformate (4.27 g, 25.03 mmol) is slowly added dropwise to 1-(4-aminophenyl)pyrrolidin-2-one (4 g, 22.7 mmol) and N,N-dimethylaniline (3.6 ml, 28.4 mmol) in tetrahydrofuran (107 ml). The reaction mixture is stirred at −20° C. for 30 min and then warmed to room temperature. After addition of ethyl acetate (0.5 l), the organic phase is washed with saturated NaCl solution (0.5 l). The combined organic phase are dried (magnesium sulfate), filtered and concentrated under reduced pressure. The residue is titrated with diethyl ether and filtered off with suction. Yield: 5.2 g, 74% of theory, light-beige crystals, melting point: 174° C.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07582666B2 |
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| 출처 데이터셋 | uspto-grants-2009_09 |
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| ORD ID | ord-e3f8471f3bc24864ab0a6bc60f92aeb9 |
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| 출처 메모 | uspto-grants-2009_09 |
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