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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 552584생성일: 2026년 10월 26일

Nicotinic Acid → (6-Hydroxy-pyridin-3-yl)-(S)(+)-(2-pyrrolidin-1-ylmethyl-pyrrolidin-1-yl)-methanone

https://huagongshe.com/reaction/552584

반응식

참여 물질

역할이름HCID투입량
반응물Nicotinic AcidHCID 938—
반응물TriethylamineHCID 8471—
반응물1-HydroxybenzotriazoleHCID 75771—
반응물CarbodiimideHCID 160435—
반응물(S)-(+)-1-(2-Pyrrolidinylmethyl)pyrrolidineHCID 853152—
용매CHCl3 BuOH MeCNHCID 131728932—
생성물(6-Hydroxy-pyridin-3-yl)-(S)(+)-(2-pyrrolidin-1-ylmethyl-pyrrolidin-1-yl)-methanoneHCID 17851972473%

반응 단계

PS-carbodiimide (1.39 mmol/g) resin beads (2.1 g, 3 mmol) are added to a 10 mL CHCl3/BuOH/MeCN (5:1:1) mixture of nicotinic acid (278 mg, 2 mmol), (S)(+)-1-(2-pyrrolidinylmethyl)pyrrolidine (231 mg, 1.5 mmol), HOBt (300 mg, 2.2 mmol), and triethylamine (0.30 mL, 2.2 mmol). The mixture is shaken at room temperature for 3 days. The reaction mixture is filtered and the beads are washed alternately with MeOH, then CH2Cl2, and the filtrate is concentrated in vacuo. The crude material product is partially purified by a SCX column (MeOH wash, elution with 2M NH3 in MeOH. Further purification is accomplished using silica-gel column chromatography (gradient: 100% CH2Cl2 to 10% 2M NH3 in MeOH/CH2Cl2) to give the title compound (200 mg, 73%). MS (ES+) 276.1 (M+H)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07951826B2
출처 데이터셋uspto-grants-2011_05
ORD IDord-31969ee1edb848ccac5c2bc1371d3bec
출처 메모uspto-grants-2011_05