Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 10972생성일: 2026년 10월 25일
Methyl iodide → 3-benzyloxycarbonylamino-6-methyl-4-oxo-4,6,7,8-tetrahydro-pyrrolo[1,2-a]pyrimidine-6-carboxylic Acid tert-butyl Ester
https://huagongshe.com/reaction/10972
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Methyl iodide | HCID 6328 | — |
| 반응물 | tert-Butyl (S)-3-{[(benzyloxy)carbonyl]amino}-4-oxo-4,6,7,8-tetrahydropyrrolo[1,2-a]pyrimidine-6-carboxylate | HCID 54224046 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 3-benzyloxycarbonylamino-6-methyl-4-oxo-4,6,7,8-tetrahydro-pyrrolo[1,2-a]pyrimidine-6-carboxylic Acid tert-butyl Ester | HCID 69600879 | 160.9% |
반응 단계
To a solution of intermediate 1g (200 mg, 0.519 mmol) in 5 mL THF at −78° C., was added a 1M solution of LIHMDS in THF (1.09 mL, 1.09 mmol). The mixture was stirred for 5 min, then MeI (162 mL, 2.60 mmol) was added. The mixture was stirred with warming to −30° C. over 1 h, then was quenched with sat. NH4Cl. The mixture was diluted with EtOAc and washed with H2O and brine, dried (Na2SO4), and concentrated. The resultant residue was combined with additional crude material from another batch for purification by flash chromatography (stepwise gradient, 40 to 45 to 50% EtOAc/hexanes) to afford 59 mg of intermediate 19a (18%, based on 0.835 mmol of starting material). LR MS.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07094783B2 |
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| 출처 데이터셋 | uspto-grants-2006_08 |
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| ORD ID | ord-6dbb075c2b7a4f469c22e0890a95e7e6 |
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| 출처 메모 | uspto-grants-2006_08 |
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