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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 627129생성일: 2026년 10월 24일

(2S,5R)-tert-butyl 5-(N-(allyloxy)-2-nitrophenylsulfonamido)-2-carbamoyl-3-methyl-5,6-dihydropyridine-1(2H)-carboxylate → (2S,5R)-5-(N-(allyloxy)-2-nitrophenylsulfonamido)-3-methyl-1,2,5,6-tetrahydropyridine-2-carboxamide

https://huagongshe.com/ko/reaction/627129

반응식

참여 물질

역할이름HCID투입량
반응물(2S,5R)-tert-butyl 5-(N-(allyloxy)-2-nitrophenylsulfonamido)-2-carbamoyl-3-methyl-5,6-dihydropyridine-1(2H)-carboxylateHCID 89852450—
촉매Zinc bromideHCID 10421208—
용매DichloromethaneHCID 6344—
생성물(2S,5R)-5-(N-(allyloxy)-2-nitrophenylsulfonamido)-3-methyl-1,2,5,6-tetrahydropyridine-2-carboxamideHCID 8985208891%

반응 단계

(2S,5R)-tert-butyl 5-(N-(allyloxy)-2-nitrophenylsulfonamido)-2-carbamoyl-3-methyl-5,6-dihydropyridine-1(2H)-carboxylate (Intermediate 83, 2.785 g, 5.61 mmol) and zinc(II) bromide (2.53 g, 11.22 mmol) was added DCM (10 mL) and stirred at rt overnight. The reaction mixture was diluted with dichloromethane and washed with saturated sodium bicarbonate and brine. The organics were dried over magnesium sulfate, filtered and concentrated to afford the desired product (2.015 g, 91%) as a beige foam.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09309245B2
출처 데이터셋uspto-grants-2016_04
ORD IDord-bb8cd7d1b8094c849b4cf50c21b64855
출처 메모uspto-grants-2016_04