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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1917132생성일: 2026년 10월 25일

7-Amino-4-(2-(dimethylamino)ethyl)-2H-benzo[b][1,4]oxazin-3(4H)-one → HCID 178483725, 화합물

https://huagongshe.com/reaction/1917132

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참여 물질

역할이름HCID투입량
반응물7-Amino-4-(2-(dimethylamino)ethyl)-2H-benzo[b][1,4]oxazin-3(4H)-oneHCID 24253307—
반응물Methyl thiophene-2-carbimidothioate hydroiodideHCID 66704664—
용매EthanolHCID 702—
용매Sodium BicarbonateHCID 516892—
생성물HCID 178483725HCID 17848372588%

반응 단계

A solution of 7-amino-4-(2-(dimethylamino)ethyl)-2H-benzo[b][1,4]oxazin-3(4H)-one (0.125 g, 0.531 mmol) in dry ethanol (10 mL) was treated with methyl thiophene-2-carbimidothioate hydroiodide (0.3 g, 1.062 mmol) at room temperature and stirred overnight (18 hours). At this time, additional methyl thiophene-2-carbimidothioate hydroiodide (0.3 g, 1.062 mmol) was added, and stirring was continued for another 24 hours. The reaction was diluted with saturated NaHCO3 solution (20 mL), and the product was extracted into CH2Cl2 (2×20 mL). The combined CH2Cl2 layers were washed with brine (15 mL) and dried (Na2SO4). The solvent was evaporated, and the crude material was purified by column chromatography (5:95 (2M NH3 in MeOH):CH2Cl2) to obtain the title compound 5 (0.16 g, 88%) as a solid. 1H NMR (DMSO-d6) δ 2.19 (s, 6H), 2.43 (t, 2H, J=6.9 Hz), 3.97 (t, 2H, J=6.9 Hz), 4.58 (s, 2H), 6.48-6.58 (m, 4H), 7.06-7.14 (m, 2H), 7.60 (d, 1H, J=5.1 Hz), 7.74 (d, 1H, J=3.3 Hz); ESI-MS (m/z, %): 345 (MH+, 100), 128 (85); ESI-HRMS calculated for C17H21N4O2S (MH+), calculated: 345.1379; observed: 345.1384; HPLC-purity: 93.15% by area.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08618286B2
출처 데이터셋uspto-grants-2013_12
ORD IDord-40834211b92745a5b1d93cfd7f6fcf8e
출처 메모uspto-grants-2013_12