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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 391331생성일: 2026년 10월 24일

Methyl iodide → HCID 59578436, 화합물

https://huagongshe.com/ko/reaction/391331

반응식

참여 물질

역할이름HCID투입량
반응물Methyl iodideHCID 6328—
반응물3-Bromo-4-chloropyridineHCID 817696—
반응물Lithium diisopropylamideHCID 2724682—
반응물N-(cyclopropylmethylene)methanesulfonamideHCID 66788560—
반응물ButyllithiumHCID 178418339—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
생성물HCID 59578436HCID 59578436—

반응 조건

온도-78 °C

반응 단계

To a solution of DIPA (1.71 mL, 12 mmol) in THF (50 mL) at −78° C. was added 1.6M BuLi (7.5 mL, 12.0 mmol) and the mixture was stirred at −78° C. for 2 h. The LDA solution was cannulated into a solution of 3-bromo-4-chloropyridine (2.117 g, 11 mmol) in THF (50 mL) at −78° C., and the mixture was stirred at −78° C. for 1 h. A solution of N-(cyclopropylmethylene)methanesulfonamide (10 mmol, crude mixture) in THF (50 mL) was added and the mixture was stirred at −78° C. for 1 h. A solution of MeI (0.625 mL, 10 mmol) in THF (10 mL) was added, and the mixture was warmed to room temperature and stirred overnight. Water (0.5 mL) was added and the mixture was concentrated in vacuo. The residue was purified by silica gel chromatography eluting with a 0-50% EtOAc-heptane gradient to give N-((5-bromo-4-chloropyridin-3-yl)(cyclopropyl)methyl)-N-methylmethanesulfonamide. MS (ESI): m/z 353.0, 355.0 (M+H)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08383827B2
출처 데이터셋uspto-grants-2013_02
ORD IDord-4d2480c9553a40798ecae9f1c0e51ad7
출처 메모uspto-grants-2013_02