Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 526891생성일: 2026년 10월 26일
Sodium methanolate methanol → (S)-tetrahydrofuran-3-yl 3-(2-(5-chloro-1H-pyrrolo[2,3-b]pyridin-3-yl)-5-fluoropyrimidin-4-ylamino)azetidine-1-carboxylate
https://huagongshe.com/reaction/526891
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Sodium methanolate methanol | HCID 23694274 | — |
| 반응물 | (S)-tetrahydrofuran-3-yl 3-(2-(5-chloro-1-tosyl-1H-pyrrolo[2,3-b]pyridin-3-yl)-5-fluoropyrimidin-4-ylamino)azetidine-1-carboxylate | HCID 67287100 | — |
| 용매 | Methanol | HCID 887 | — |
| 생성물 | (S)-tetrahydrofuran-3-yl 3-(2-(5-chloro-1H-pyrrolo[2,3-b]pyridin-3-yl)-5-fluoropyrimidin-4-ylamino)azetidine-1-carboxylate | HCID 68007196 | 55% |
반응 단계
(S)-tetrahydrofuran-3-yl 3-(2-(5-chloro-1-tosyl-1H-pyrrolo[2,3-b]pyridin-3-yl)-5-fluoropyrimidin-4-ylamino)azetidine-1-carboxylate, 6d, was dissolved in methanol (2 mL) and then treated with of 25% sodium methoxide/methanol (0.5 mL) and heated at 60° C. in sealed tube. LCMS showed complete reaction after 10 minutes. The resulting solution was quenched with aqueous saturated NH4Cl solution (0.5 mL) then evaporated to dryness and the residue dissolved in DMSO and purified by reverse phase HPLC (ammonium formate buffer) to afford 25.9 mg (55% yield) of the desired product, 422, as a solid.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US09345708B2 |
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| 출처 데이터셋 | uspto-grants-2016_05 |
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| ORD ID | ord-3dc9bcaf090543bc9c50cf17c5763dac |
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| 출처 메모 | uspto-grants-2016_05 |
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