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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1715286생성일: 2026년 10월 27일

Triethylamine → N,N-dimethyl-N~2~-({[4'-methyl-2-(morpholin-4-ylcarbonyl)-4,5'-bi-1,3-thiazol-2'-yl]amino}carbonyl)glycinamide

https://huagongshe.com/reaction/1715286

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물2-Amino-N,N-dimethylacetamide acetateHCID 53399009—
반응물N-[4'-methyl-2-(morpholin-4-ylcarbonyl)-4,5'-bi-1,3-thiazol-2'-yl]-1H-imidazole-1-carboxamideHCID 59465567—
용매DimethylformamideHCID 6228—
생성물N,N-dimethyl-N~2~-({[4'-methyl-2-(morpholin-4-ylcarbonyl)-4,5'-bi-1,3-thiazol-2'-yl]amino}carbonyl)glycinamideHCID 1199010860%

반응 단계

To N-[4′-methyl-2-(morpholin-4-ylcarbonyl)-4,5′-bi-1,3-thiazol-2′-yl]-1H-imidazole-1-carboxamide, prepared as in Step 3 of Example 36, described above (75 mg; 0.19 mmol; 1 eq.) is added DMF (3 ml), glycine dimethylamide acetate (Chem-Impex) (30.1 mg; 0.19 mmol; 1 eq.) and triethylamine (57 μl; 0.41 mmol; 2.20 eq.). The mixture is stirred 3 hours at rt. Solvents are evaporated and the crude product is crystallized in MeOH, affording Compound (46) as a light yellow solid (49 mg; 60%). 1H NMR (DMSO-d6, 300 MHz) δ 2.44 (s, 3H), 2.86 (s, 3H), 2.94 (s, 3H), 3.68 (m, 6H), 4.01 (m, 2H), 4.33 (m, 2H), 6.83 (m, 1H), 7.91 (s, 1H), 10.70 (br s, 1H). M− (ESI): 437.15; M+ (ESI): 439.09. HPLC (method A), Rt: 2.30 min (purity: 99%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07799814B2
출처 데이터셋uspto-grants-2010_09
ORD IDord-677a61ddda72456e955578dca060b746
출처 메모uspto-grants-2010_09