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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2068291Generated: November 1, 2026

N-(1-(4-(tert-butyldimethylsilyloxy)cyclohexyl)-5-((4-(2-(pyridin-4-yl)ethyl)piperazin-1-yl)methyl)-1H-benzo[d]imidazol-2-yl)-5-(4-methoxypyridin-3-yl)-1-((2-(trimethylsilyl)ethoxy)methyl)-1H-indazol-3-amine → HCID 24798636, compound

https://huagongshe.com/reaction/2068291

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-(1-(4-(tert-butyldimethylsilyloxy)cyclohexyl)-5-((4-(2-(pyridin-4-yl)ethyl)piperazin-1-yl)methyl)-1H-benzo[d]imidazol-2-yl)-5-(4-methoxypyridin-3-yl)-1-((2-(trimethylsilyl)ethoxy)methyl)-1H-indazol-3-amineHCID 86654792—
SolventHydrochloric AcidHCID 313—
ProductHCID 24798636HCID 2479863637.1%

Reaction Steps

In a 20 mL vial was added N-(1-(4-(tert-butyldimethylsilyloxy)cyclohexyl)-5-((4-(2-(pyridin-4-yl)ethyl)piperazin-1-yl)methyl)-1H-benzo[d]imidazol-2-yl)-5-(4-methoxypyridin-3-yl)-1-((2-(trimethylsilyl)ethoxy)methyl)-1H-indazol-3-amine (31 mg, 0.000034 mol) ethanol (1.20 mL) and 0.01M hydrogen chloride (300 uL). The reaction mixture was brought to reflux and maintained at reflux for 1 hour. The reaction mixture was concentrated to a brownish residue and purified by HPLC yielding 8.3 mg of the title compound as the bis TFA salt as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08293923B2
Source datasetuspto-grants-2012_10
ORD IDord-221f497e35d74f2a83e0efdccfe942c4
Source noteuspto-grants-2012_10