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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 364445생성일: 2026년 10월 24일

Ethylmorpholine → N-[[6-methoxy-5-(pentafluoroethyl)-1-naphthalenyl]carbonyl]-N-methylglycine, methyl ester

https://huagongshe.com/ko/reaction/364445

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참여 물질

역할이름HCID투입량
반응물EthylmorpholineHCID 7525—
반응물DicyclohexylcarbodiimideHCID 10868—
반응물1-HydroxybenzotriazoleHCID 75771—
반응물Glycine, N-methyl-, methyl ester, hydrochloride (1:1)HCID 83544—
반응물6-Methoxy-5-(pentafluoroethyl)naphthalene-1-carboxylic acidHCID 13959076—
용매DimethylformamideHCID 6228—
생성물N-[[6-methoxy-5-(pentafluoroethyl)-1-naphthalenyl]carbonyl]-N-methylglycine, methyl esterHCID 13171482154.1%

반응 단계

The crude 6-methoxy-5-(pentafluoroethyl)-1-naphthalene carboxylic acid (3.65 g, 11.4 mmol), 1-hydroxybenzotriazole (2.31 g, 17.1 mmol), dry distilled dimethylformamide (35 ml) and dicyclohexylcarbodiimide (2.82 g, 13.7 mmol) were stirred at room temperature for 1 hour. The mixture was cooled to 0° C., a solution of sarcosine methyl ester hydrochloride (3.18 g, 22.8 mmol) in dimethylformamide (30 ml) and N-ethyl morpholine (2.92 ml, 22.8 mmol) was added and stirring continued for 2 hours at room temperature. After cooling to 0° C., the precipitate (dicyclohexyl urea) was removed by filtration, the filtrate evaporated and the residue purified by HPLC (ethyl acetate/hexane 1:1, Waters Prep LC 500A). 1.5 g of pure, and 2.5 g of less pure N-[[6-methoxy-5-(pentafluoroethyl)-1-naphthalenyl]carbonyl]-N-methylglycine, methyl ester were obtained. nmr (DMSO): δ2.75 & 3.25 (2s, 3H, N--CH3, rotamers); δ3.75 (s, 3H, OCH3); δ3.97 (s, 3H, OCH3); δ4.35 (broad, 2H, N--CH2 --CO); δ7.7 (m, 5H, Har). ms: m/e 405 (M+), 303, 195, 102.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04604406
출처 데이터셋uspto-grants-1986_08
ORD IDord-bc8ee403baaf4b9e8c8eaf8efd63030c
출처 메모uspto-grants-1986_08