돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 634510생성일: 2026년 10월 24일

Acetic Acid → 3-(1-(4-amino-3-(3-fluoro-5-hydroxyphenyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl)ethyl)-4-(3-(dimethylamino)prop-1-yn-1-yl)-1H-isochromen-1-one hydrochloride

https://huagongshe.com/ko/reaction/634510

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물DichloromethaneHCID 6344—
반응물N,N-DiisopropylmethylamineHCID 547370—
반응물Sodium triacetoxyborohydrideHCID 5049666—
반응물CID 19593658HCID 19593658—
반응물Benzyl (3-(3-(1-(4-amino-3-(3-fluoro-5-methoxyphenyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl)ethyl)-1-oxo-1H-isochromen-4-yl)prop-2-yn-1-yl)(methyl)carbamateHCID 118150098—
용매EthanolHCID 702—
용매Boron tribromideHCID 25134—
생성물3-(1-(4-amino-3-(3-fluoro-5-hydroxyphenyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl)ethyl)-4-(3-(dimethylamino)prop-1-yn-1-yl)-1H-isochromen-1-one hydrochlorideHCID 1181315156.37%

반응 조건

온도0 °C

반응 단계

To a solution of benzyl (3-(3-(1-(4-amino-3-(3-fluoro-5-methoxyphenyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl)ethyl)-1-oxo-1H-isochromen-4-yl)prop-2-yn-1-yl)(methyl)carbamate (100 mg, 0.158 mmol) in DCM (4 ml), 1M BBr3 in DCM (3 ml, 10.50 mmol) was added and the reaction was stirred overnight. Then, the solution was cooled to 0° C. and stirred for 1 h. Then, EtOH (1 ml) was added and solvent was removed under reduced. The resulting material was reacted in DCM (4 ml) with trioxane (0.049 ml, 0.472 mmol), N-isopropyl-N-methylpropan-2-amine (18.14 mg, 0.157 mmol) for 30 min. Then, sodium triacetoxyborohydride (100 mg, 0.472 mmol) and acetic acid (28.4 mg, 0.472 mmol) were added and the reaction stirred for 1 h. Solvent was removed and crude was purified by C18 flash chromatography ((H2O/ACN)) 95:5+0.1% HCOOH}:{(ACN/H2O) 95:5+HCOOH 0.1%} from 100:0 to 0:100 affording the title compound (5 mg, 10.03 mmol, 6.37% yield) as a white solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09321776B2
출처 데이터셋uspto-grants-2016_04
ORD IDord-344db73ad0494d4195585ea9df0eed89
출처 메모uspto-grants-2016_04