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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2202597생성일: 2026년 10월 26일

Acetonitrile → Ethyl 6-((R)-3-benzhydryloxypyrrolidin-1-ylmethyl)pyridine-2-carboxylate

https://huagongshe.com/reaction/2202597

반응식

참여 물질

역할이름HCID투입량
반응물AcetonitrileHCID 6342—
반응물TriethylamineHCID 8471—
반응물Ethyl 6-(chloromethyl)pyridine-2-carboxylateHCID 15614003—
반응물(R)-3-benzhydryloxypyrrolidineHCID 70647884—
용매Ethyl AcetateHCID 8857—
생성물Ethyl 6-((R)-3-benzhydryloxypyrrolidin-1-ylmethyl)pyridine-2-carboxylateHCID 8668028954%

반응 단계

A mixture of 8.144 g of (R)-3-benzhydryloxypyrrolidine synthesized in Production Example 168, 7.701 g of a known compound ethyl 6-chloromethylpyridine-2-carboxylate, 69 mL of acetonitrile, and 9.0 mL of triethylamine was heated under reflux for 3 hours. After being allowed to cool down, the mixture was diluted with ethyl acetate. The diluted mixture was poured into a saturated saline solution, and the organic layer was collected by separation. The organic layer was washed with a saturated saline solution and dried over magnesium sulfate. The solvent was distilled off, and then the residue was purified by silica gel column chromatography (chloroform/acetone (volume ratio)=15:1 to 10:1) to give the title compound (7.22 g (54%)).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09365553B2
출처 데이터셋uspto-grants-2016_06
ORD IDord-87ead9f29d3c44d09a18ab4650c96571
출처 메모uspto-grants-2016_06