HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2119339Generated: November 2, 2026
Diisopropylethylamine → HCID 23440705, compound
https://huagongshe.com/reaction/2119339
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | PyBroP | HCID 2733179 | — |
| Reactant | HCID 9930132 | HCID 9930132 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Dichloromethane methanol | HCID 21226129 | — |
| Product | HCID 23440705 | HCID 23440705 | — |
Reaction Steps
6-(2,3-Dihydro-benzofuran-5-yl)-2-methyl-2,3,6,7,12,12a-hexahydro pyrazino[1′,2′:1,6]pyrido[3,4-b]indole-1,4-dione (39.6 mg, 0.1019 mmol), prepared according to Example 1 or 2 as described in WO97/03675, was dissolved in DMF (1.0 mL). To the solution was added KOt-Bu (0.173 mL, 1.0 M in THF). The solution was stirred under air (passed through drying tube) for 3 hours. Additional KOt-Bu (0.15 mL, 1.0 M in THF) was added and the reaction mixture stirred for another 3 hours under dry air. The reaction mixture was quenched by HCl (0.323 mL, 1.0 M HCl in ether) and the ether solvent evaporated. PyBrOP (53 mg, 0.1019 mmol) and DIPEA (0.036 mL, 0.204 mmol) were added, then DMF (0.2 mL) was added to make the total volume 1 mL. The resulting mixture was stirred at room temperature for 16 hours. Preparative TLC (1% CH3OH/CH2Cl2) yield the title product as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06686349B2 |
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| Source dataset | uspto-grants-2004_02 |
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| ORD ID | ord-aeeb40cf30d04457899af43463d7c982 |
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| Source note | uspto-grants-2004_02 |
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