HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1639009Generated: October 31, 2026
Potassium Hydroxide → HCID 14622474, compound
https://huagongshe.com/reaction/1639009
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 14622449 | HCID 14622449 | — |
| Reactant | HCID 178527775 | HCID 178527775 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 14622474 | HCID 14622474 | 60.4% |
Reaction Steps
To a solution of 514.8 mg of 86% KOH (7.87 mmol) in 20 ml of 99% EtOH were added 434.1 mg of 2-mercaptobenzimidazole (II-1) (2.89 mmol) and 900.1 mg of 1-dichloromethyl-6-methoxy-7-(2,2,2-trifluoroethoxy)-3,4-dihydroisoquinoline (IV-1) (2.63 mmol) in order. After stirring for 30 min. at room temperature, the mixture was refluxed for 3 hr. and concentrated under reduced pressure. The residue was mixed with water and extracted with CHCl3. The objective compound existing as an insoluble material was filtered and combined with CHCl3 extract to give 722.5 mg of the crude product. It was dispersed in 15 ml of CH2Cl2, filtered and washed with CH2Cl2 to give 666.5 mg of the titled compound 2-{[6-methoxy-7-(2,2,2-trifluoroethoxy)isoquinolin-1-yl]methylthio}-benzimidazole (Ia-7) (Yield: 60.4%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04882338 |
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| Source dataset | uspto-grants-1989_11 |
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| ORD ID | ord-8885082bd95246b8880644c6c16c6c02 |
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| Source note | uspto-grants-1989_11 |
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