Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 634510Generated: October 25, 2026

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/reaction/634510

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantDichloromethaneHCID 6344—
ReactantN,N-DiisopropylmethylamineHCID 547370—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantCID 19593658HCID 19593658—
ReactantBenzyl (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—
SolventEthanolHCID 702—
SolventBoron tribromideHCID 25134—
Product3-(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%

Reaction Conditions

Temperature0 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09321776B2
Source datasetuspto-grants-2016_04
ORD IDord-344db73ad0494d4195585ea9df0eed89
Source noteuspto-grants-2016_04