Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 730408생성일: 2026년 10월 24일
4-Methylmorpholine → tert-butyl N-{4'-[3-(N'-butyrylhydrazino)-2-ethoxy-3-oxopropyl]biphenyl-3-ylmethyl}-N-methylcarbamate
https://huagongshe.com/ko/reaction/730408
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 4-Methylmorpholine | HCID 7972 | — |
| 반응물 | Ethyl Acetate | HCID 8857 | — |
| 반응물 | Diisopropylcarbodiimide | HCID 12734 | — |
| 반응물 | 1-Hydroxybenzotriazole | HCID 75771 | — |
| 반응물 | Butyrohydrazide | HCID 77079 | — |
| 반응물 | 3-{3'-[(Tert-butoxycarbonylmethylamino)methyl]biphenyl-4-yl}-2-ethoxypropionic acid | HCID 68852083 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | tert-butyl N-{4'-[3-(N'-butyrylhydrazino)-2-ethoxy-3-oxopropyl]biphenyl-3-ylmethyl}-N-methylcarbamate | HCID 68852131 | 100% |
반응 단계
0.15 ml (1.33 mmol) of N-methylmorpholine is added to a solution of 0.5 g (1.2 mmol) of 3-{3′-[(tert-butoxycarbonylmethylamino)methyl]biphenyl-4-yl}-2-ethoxypropionic acid, 0.14 g (1.3 mmol) of butyric hydrazide and 0.33 g (2.4 mmol) of 1-hydroxybenzotriazole in 10 ml of tetrahydrofuran cooled to −5° C. After stirring for 5 minutes, 0.2 ml (1.3 mmol) of diisopropylcarbodiimide is added. The reaction medium is stirred at 0° C. for 1 hour and then at room temperature for 2 hours, diluted with ethyl acetate, washed with saturated aqueous caesium hydrogen carbonate solution, extracted with ethyl acetate, dried over magnesium sulfate, filtered and concentrated. The residue obtained is chromatographed on a column of silica eluted with a 1/1 heptane/ethyl acetate mixture. 0.6 g of tert-butyl N-{4′-[3-(N′-butyrylhydrazino)-2-ethoxy-3-oxopropyl]biphenyl-3-ylmethyl}-N-methylcarbamate is obtained in a yield of 100%.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07582663B2 |
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| 출처 데이터셋 | uspto-grants-2009_09 |
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| ORD ID | ord-232fb9bc676e4d25827e2f4eb22ebbce |
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| 출처 메모 | uspto-grants-2009_09 |
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