HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1625010Generated: October 31, 2026
Benzenemethanamine, 3,4-dichloro- → HCID 24805212, compound
https://huagongshe.com/reaction/1625010
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzenemethanamine, 3,4-dichloro- | HCID 1608 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| Reactant | HCID 58270431 | HCID 58270431 | — |
| Catalyst | Molybdenum carbonyl (Mo(CO)6) | HCID 98885 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Product | HCID 24805212 | HCID 24805212 | — |
Reaction Steps
A 5-mL process vial was charged with 2-cyclopropyl-5-iodoisoquinolin-1(2H)-one (100 mg, 0.0004 mol), 3,4-dichloro-benzylamine (200 mg, 0.001 mol), molybdenum hexacarbonyl (90 mg, 0.0004 mol), palladium acetate (8 mg, 0.00004 mol), 1,8-diazabicyclo[5.4.0]undec-7-ene (200 mg, 0.001 mol) and 1,4-dioxane (2 mL, 0.02 mol). The vessel was sealed under air and exposed to microwave heating for 15 min at 110° C. The reaction tube was thereafter cooled to room temperature, and the mixture was concentrated and dissolved in a small volume of dichloromethane. The crude product was purified via flash column chromatography (12 g of silica gel, 50% EtOAC/Hexane) and then prep. HPLC to give the desired product as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08779144B2 |
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| Source dataset | uspto-grants-2014_07 |
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| ORD ID | ord-ffc76557d1414adda89b36148284dad3 |
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| Source note | uspto-grants-2014_07 |
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