HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 881993Generated: November 2, 2026
Dimethylformamide → HCID 56933724, compound
https://huagongshe.com/reaction/881993
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 6,7-Dimethoxy-1,2,3,4-Tetrahydroisoquinoline | HCID 15623 | — |
| Reactant | HCID 86691333 | HCID 86691333 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 56933724 | HCID 56933724 | 75% |
Reaction Steps
(3-(tosylmethyl)-5-methyl-2-methylenehexyl)trimethylsilane (Formula 4; 72.0 mg, 0.195 mmol) and Na2CO3 (41.4 mg, 0.391 mmol) were added to DMF (2 mL). Then, 6,7-dimethoxy-1,2,3,4-tetrahydroisoquinoline (Formula 3; 75.4 mg, 0.391 mmol) was added thereto, and the mixture was heated up to 80° C. and stirred for 30 hr. Distilled water was put into the reaction solution to complete the reaction, and then the temperature was increased to normal temperature. An organic layer was extracted, the organic layer collected was washed with distilled water and a brine solution, and the remaining solvent was distilled under reduced pressure. Anhydrous magnesium sulfate was used to dry the organic layer, filtration under reduced pressure and evaporation under reduced pressure were performed, and then column chromatography was used to obtain 53.3 mg (yield 75%) of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08993766B2 |
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| Source dataset | uspto-grants-2015_03 |
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| ORD ID | ord-f632e2cf6145427eb19bb628fb18c6fc |
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| Source note | uspto-grants-2015_03 |
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