HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2174061Generated: October 30, 2026
HCID 86701687, compound → HCID 178437481, compound
https://huagongshe.com/reaction/2174061
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 86701687 | HCID 86701687 | — |
| Reactant | HCID 86701688 | HCID 86701688 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 178437481 | HCID 178437481 | — |
Reaction Steps
A solution of a mixture of 2-(1-(5-ethyl-7-methyl-1-tosyl-1H-indol-4-yl)vinyl)-1-((2-(trimethylsilyl)ethoxy)methyl)-1H-benzo[d]imidazole-5-carbonitrile and 2-(1-(5-ethyl-7-methyl-1-tosyl-1H-indol-4-yl)vinyl)-1-((2-(trimethylsilyl)ethoxy)methyl)-1H-benzo[d]imidazole-6-carbonitrile (100 mg, 0.164 mmol) in 1M HCl in MeOH (10 mL) was stirred at 60° C. for 5 h. The reaction mixture was cooled to room temperature. The reaction mixture was 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 any further purification. MS (ESI+) m/z 481.2 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09056874B2 |
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| Source dataset | uspto-grants-2015_06 |
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| ORD ID | ord-9952122de84045fc92410c312f3aea35 |
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| Source note | uspto-grants-2015_06 |
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