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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2217310Generated: October 31, 2026

Potassium Carbonate → HCID 69321501, compound

https://huagongshe.com/reaction/2217310

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantAmmonium HydroxideHCID 14923—
ReactantBoron tribromideHCID 25134—
ReactantHCID 22037010HCID 22037010—
SolventDichloromethaneHCID 6344—
ProductHCID 69321501HCID 69321501146.4%

Reaction Conditions

Temperature0 °C

Reaction Steps

(±)-N-[1-(2-amino-3-methylbutyl)-4-piperidinyl]-1-[(5,6,7,8-tetrahydro-3-methoxy-2-quinolinyl)methyl]-1H-benzimidazol-2-amine tetrahydrochloride monohydrate (0.00218 mol) was basified with K2CO3 10%. The mixture was extracted with CH2Cl2. The organic layer was separated, dried (MgSO4), filtered and the solvent was evaporated, to give A′. A mixture of A′ in dichloromethane (50 ml) was cooled to 0° C. A solution of tribromoborane in dichloromethane (0.01526 mol) was added dropwise. The mixture was stirred at room temperature overnight, poured out on ice, basified with a concentrated NH4OH solution, decanted and extracted with CH2Cl2. The organic layer was separated, dried (MgSO4), filtered and the solvent was evaporated. The residue (1.1 g) was purified by column chromatography over silica gel (eluent: CH2Cl2/CH3OH/NH4OH 90/10/0.5; 20-45 μm). The desired fractions were collected and the solvent was evaporated. The residue was converted into the hydrochloric acid salt (1:4) with HCl/2-propanol. The precipitate was filtered off and dried, yielding 0.5 g (37%) of (±)-N-[1-(2-amino-3-methylbutyl)-4-piperidinyl]-1-[(5,6,7,8-tetrahydro-3-hydroxy-2-quinolinyl)methyl]-1H-benzimidazol-2-amine tetrahydro-chloride monohydrate; mp. 240° C. (comp. 63).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07407969B2
Source datasetuspto-grants-2008_08
ORD IDord-fd7ed0a3c87f418796d52a300989e565
Source noteuspto-grants-2008_08