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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1449990Generated: October 31, 2026

Sodium Bicarbonate → HCID 178521182, compound

https://huagongshe.com/reaction/1449990

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
Reactant2-Bromo-1-(1,2,3,4-tetrahydroisoquinolin-2-yl)ethan-1-oneHCID 18467239—
ReactantHCID 178505426HCID 178505426—
SolventAcetonitrileHCID 6342—
ProductHCID 178521182HCID 17852118255.3%

Reaction Steps

To a solution of 4-(6-fluoro-1H-indazol-3-yl)piperidine (4.8 g, 18.9 mmol) in CH3CN (200 ml) was added 2-bromo-1-(1,2,3,4-tetrahydroisoquinolin-2-yl)ethanone (4.8 g, 18.9 mmol) and sodium bicarbonate (1.9 g, 22.7 mmol) at room temperature. The reaction mixture was warmed to reflux (4 hours), cooled to room temperature and filtered through a pad of celite. The solids were washed with DCM and the combined filtrates were concentrated. The remaining residue was purified via preparative HPLC (silica gel, 5-10% MeOH/DCM) to give 4.1 g of 1-(1,2,3,4-tetrahydroisoquinolin-2-yl)-2-[4-(6-fluoro-1H-indazol-3-yl)-1-piperidinyl]ethanone which was used without further purification. To a suspension of the latter (3.7 g, 9.4 mmol) in THF (100 ml) was added (dropwise) lithium aluminum hydride (11.3 ml of 1.0M solution in THF, 11.3 mmol) at room temperature, under nitrogen. The reaction mixture was warmed to reflux (5 hours), cooled to room temperature and carefully quenched with water (10 ml). The precipitated salts were removed via filtration and washed with 1:1 EtOAc/DCM. The combined filtrates were concentrated and the remaining oil was purified via flash column chromatography (silica gel, 10% MeOH/DCM) to give 2.2 g of the product. The dimaleate salt was prepared in methanol (30 ml) with maleic acid (3.0 eq.), m.p. 185°-187° C. ANALYSIS: Calculated for C23H27FN4.2C4H4O4 : 60.98%C 5.78%H 9.18%N Found: 60.85%C 5.75%H 9.09%N

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05599821
Source datasetuspto-grants-1997_02
ORD IDord-1628abc50def4e7ba6e1ce4c201b78f4
Source noteuspto-grants-1997_02