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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 219969생성일: 2026년 10월 23일

Glycine, N-methyl-, methyl ester, hydrochloride (1:1) → Methyl N-(3-{5-[2-(methoxymethyl)-2'-methylbiphenyl-4-yl]-1,2,4-oxadiazol-3-yl}benzoyl)-N-methylglycinate

https://huagongshe.com/ko/reaction/219969

반응식

참여 물질

역할이름HCID투입량
반응물Glycine, N-methyl-, methyl ester, hydrochloride (1:1)HCID 83544—
반응물3-{5-[2-(Methoxymethyl)-2'-methylbiphenyl-4-yl]-1,2,4-oxadiazol-3-yl}benzoyl chlorideHCID 86645658—
생성물Methyl N-(3-{5-[2-(methoxymethyl)-2'-methylbiphenyl-4-yl]-1,2,4-oxadiazol-3-yl}benzoyl)-N-methylglycinateHCID 59495748—

반응 단계

The title compound was prepared following procedure described in example 121 starting from 3-{5-[2-(methoxymethyl)-2′-methylbiphenyl-4-yl]-1,2,4-oxadiazol-3-yl}benzoyl chloride, prepared as in example 130, and sarcosine methyl ester hydrochloride. The title compound was obtained as a sticky solid. 1H NMR: (DMSO-d6, 300 MHz) δ 8.42 (brs, 1H), 8.28 (m, 2H), 8.17 (m, 1H), 7.61 (m, 2H), 7.34-7.22 (m, 4H), 7.12 (m, 1H), 4.32 (s, 1H), 4.22 (s, 1H), 3.80 (m, 3H), 3.32 (s, 3H), 3.1 (m, 3H). LC/MS (Method B): 486.2 (M+H)+ no (M−H)−. HPLC (Method A) Rt: 5.66 min (purity: 98.5%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08202865B2
출처 데이터셋uspto-grants-2012_06
ORD IDord-a7a5ae3ca37d4f28ba7a471fa1a5f307
출처 메모uspto-grants-2012_06