돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1875502생성일: 2026년 10월 26일

Water → 2-Amino-5,6,7,8-tetrahydro[1]benzothieno[2,3-d]pyrimidin-4(3h)-one

https://huagongshe.com/reaction/1875502

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Ammonium HydroxideHCID 14923—
반응물Ethyl 2-amino-4,5,6,7-tetrahydrobenzo[b]thiophene-3-carboxylateHCID 78262—
반응물HCID 135916071HCID 135916071—
용매Dimethyl SulfoneHCID 6213—
생성물2-Amino-5,6,7,8-tetrahydro[1]benzothieno[2,3-d]pyrimidin-4(3h)-oneHCID 29019760%

반응 조건

온도150 °C

반응 단계

To a 50 mL flask was added 4 (225 mg, 1 mmol), 9 (452 mg, 4 mmol) in DMSO2 (500 mg) was heated at 150° C. for 2 h. The mixture was cooled to room temperature. 15 mL water was added and ammonium hydroxide was used to neutralize the suspension. The brown solid was obtained by filtration. Washed with water and dried. The solid was dissolved in methanol and silica gel was added. A dry silica gel plug obtained after evaporation. The plug was then loaded on the column and washed with 5% methanol in chloroform. The fractions containing the desired product (TLC) were pooled and evaporated to afford 132 mg (60%) of 10 as a white solid: 1H NMR (DMSO-d6) δ 1.71 (m, 4H), 2.60 (m, 2H), 2.72 (m, 2H), 6.38 (s, 2H), 10.72 (s, 1H). Anal. calcd for C10H11N3OS: C, 54.28; H, 5.01; N, 18.99; 0, 7.23; S, 14.49. Found: C, 53.45; H, 5.06; N, 18.26; S, 14.02.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08309564B2
출처 데이터셋uspto-grants-2012_11
ORD IDord-f4f26fccdecc4a89bea282ad0bc7a48c
출처 메모uspto-grants-2012_11