Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1009302생성일: 2026년 10월 25일
Sodium Iodide → (2S)-2-benzyloxycarbonylamino-4-methyl-pentanoic acid 3-methyloxetan-3-ylmethyl ester
https://huagongshe.com/reaction/1009302
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Sodium Iodide | HCID 5238 | — |
| 반응물 | Cesium carbonate | HCID 10796 | — |
| 반응물 | Leucine, N-carboxy-, N-benzyl ester, L- | HCID 74840 | — |
| 반응물 | 3-Methyl-3-(toluenesulfonyl-oxymethyl)oxetane | HCID 53425830 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | (2S)-2-benzyloxycarbonylamino-4-methyl-pentanoic acid 3-methyloxetan-3-ylmethyl ester | HCID 67298758 | — |
반응 단계
Cbz-L-leucine (2 g, 7.5 mmol) and Cs2CO3 (1.46 g, 4.5 mmol, 0.6 eq) were dissolved in water (20 mL). Water was then removed in vacuo, and the resulting oil was lyophilized for 12 h to give a white solid. To this solid were added 3-methyl-3-(toluenesulfonyl-oxymethyl)oxetane (oxetane tosylate) (1.8 g, 4.5 mmol), and NaI (224 mg, 1.5 mmol, 0.2 eq.) which were taken up in DMF (35 mL) and allowed to stir under nitrogen for 48 h. The DMF was then removed in vacuo, and the resulting solid was dissolved in EtOAc (60 mL) and washed with 10% NaHCO3 (20 mL) and saturated NaCl (10 mL) and dried over MgSO4. The solvent was removed under reduced pressure to yield yellow oil which was flash column chromatographed on 200 cm3 of silica gel using 3:1 hexanes:EtOAc as an eluant to give (2S)-2-benzyloxycarbonylamino-4-methyl-pentanoic acid 3-methyloxetan-3-ylmethyl ester (Cbz-Leu oxetane ester) as a yellow thick oil.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07973037B2 |
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| 출처 데이터셋 | uspto-grants-2011_07 |
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| ORD ID | ord-e45cf123f9904c33b2bec85016ac9173 |
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| 출처 메모 | uspto-grants-2011_07 |
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