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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2174064Generated: October 29, 2026

HCID 86701692, compound → HCID 178435674, compound

https://huagongshe.com/reaction/2174064

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 86701692HCID 86701692—
ReactantHCID 86701693HCID 86701693—
SolventHydrochloric AcidHCID 313—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
ProductHCID 178435674HCID 178435674—

Reaction Conditions

Temperature60 °C

Reaction Steps

A solution of a mixture of 2-((5-ethyl-7-methyl-1-tosyl-3-(1-((2-(trimethylsilyl)ethoxy)methyl)-1H-pyrazol-5-yl)-1H-indol-4-yl)methyl)-1-((2-(trimethylsilyl)ethoxy)methyl)-1H-benzo[d]imidazole-5-carbonitrile and 2-((5-Ethyl-7-methyl-1-tosyl-3-(1-((2-(trimethylsilyl)ethoxy)methyl)-1H-pyrazol-5-yl)-1H-indol-4-yl)methyl)-1-((2-(trimethylsilyl)ethoxy)methyl)-1H-benzo[d]imidazole-6-carbonitrile (94 mg, 0.118 mmol) in 1M HCl in MeOH (5 mL) was stirred at 60° C. for 14 h. The reaction mixture was cooled to room temperature and diluted with CH2Cl2. The layers were separated and the organic phase was successively washed with 5% aq. NaHCO3, H2O and brine, dried over Na2SO4, and filtered. Concentration of the filtrate gave the title compound, without need of further purification. MS (ESI+) m/z 535.1 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09056874B2
Source datasetuspto-grants-2015_06
ORD IDord-c5d3ef86742b4b2084c829f383bb130f
Source noteuspto-grants-2015_06