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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 330203생성일: 2026년 10월 26일

Propylamine → Methyl 4-[5-(2-carboxy-1-hydroxy-3-(propylcarbamoyl)propyl]-1-propylindol-3-ylmethyl]-3-methoxybenzoate

https://huagongshe.com/reaction/330203

반응식

참여 물질

역할이름HCID투입량
반응물PropylamineHCID 7852—
반응물TriethylamineHCID 8471—
반응물Methyl 4-[5-(3-carboxy-2,3,4,5-tetrahydro-5-oxofuran-2-yl)-1-propylindol-3-ylmethyl]-3-methoxybenzoateHCID 19870632—
용매DichloromethaneHCID 6344—
용매Ethyl AcetateHCID 8857—
생성물Methyl 4-[5-(2-carboxy-1-hydroxy-3-(propylcarbamoyl)propyl]-1-propylindol-3-ylmethyl]-3-methoxybenzoateHCID 19870545—

반응 단계

A solution of methyl 4-[5-(3-carboxy-2,3,4,5-tetrahydro-5-oxofuran-2-yl)-1-propylindol-3-ylmethyl]-3-methoxybenzoate (0.89 g), triethylamine (2.1 g), and propylamine (1.5 g) in methylene chloride (15 ml) was stirred and heated under reflux for 22 hr. The cooled mixture was diluted with ethyl acetate, washed (1M hydrochloric acid (twice), water (3 times), brine), dried (MgSO4), and evaporated to give methyl 4-[5-(2-carboxy-1-hydroxy-3-(propylcarbamoyl)propyl]-1-propylindol-3-ylmethyl]-3-methoxybenzoate (0.82 g, 82%, as a mixture of diastereomers) as an off-white foam: partial NMR (300 MHz, DMSO-d6): 0.80(m, 6H, 2×CH3, both isomers), 3.83(s, 3H, OCH3, both isomers), 3.92(s, 3H, OCH3, both isomers), 4.71(d, 0.5H, CHOH, isomer A), 5.05(d, 0.5H, CHOH, isomer B), 7.64(t, 0.5H, NH isomer A/B), 7.75(t, 0.5H, NH isomer B/A).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04894386
출처 데이터셋uspto-grants-1990_01
ORD IDord-7fbc992c1416419785df3f8ee6f348a7
출처 메모uspto-grants-1990_01