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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 490120생성일: 2026년 10월 26일

Dimethylamine → tert-butyl (2S,4S)-2-(dimethylcarbamoyl)-4-hydroxypyrrolidine-1-carboxylate

https://huagongshe.com/reaction/490120

반응식

참여 물질

역할이름HCID투입량
반응물DimethylamineHCID 674—
반응물Potassium CarbonateHCID 11430—
반응물(2S,4S)-1-(tert-butoxycarbonyl)-4-hydroxypyrrolidine-2-carboxylic acidHCID 688614—
반응물1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
반응물1-Hydroxybenzotriazole hydrateHCID 2796029—
용매ChloroformHCID 6212—
용매TetrahydrofuranHCID 8028—
용매Ethyl acetate hexaneHCID 21226206—
생성물tert-butyl (2S,4S)-2-(dimethylcarbamoyl)-4-hydroxypyrrolidine-1-carboxylateHCID 6743010977.5%

반응 단계

9.95 g of 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride was added under ice cooling to a 100 mL tetrahydrofuran solution of 10.0 g of (4S)-1-(tert-butoxycarbonyl)-4-hydroxy-L-proline and 8.77 g of 1-hydroxybenzotriazole monohydrate, and the reaction mixture was stirred for 30 minutes at the same temperature. 15.6 g of a 50% dimethylamine aqueous solution was than added to the reaction solution, after which the reaction mixture was stirred for 1 hour at room temperature. 100 mL of chloroform and 50 mL of a 5% potassium carbonate aqueous solution were added to the reaction solution, liquid separation was performed, the aqueous layer was extracted with chloroform (30 mL×2), and the combined organic layer was washed with 30 mL of saturated brine and dried with magnesium sulfate, after which the drying agent was filtered off and the solvent was distilled off under reduced pressure. The residue thus obtained was subjected to column chromatography (silica gel 60, mobile phase: ethyl acetate/n-hexane=1/1 to 10/0; v/v) to obtain 8.66 g of the titled compound (colorless solid).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07528124B2
출처 데이터셋uspto-grants-2009_05
ORD IDord-fa0451fe978d46ea9a63b39814c5ade1
출처 메모uspto-grants-2009_05