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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2119339Generated: November 2, 2026

Diisopropylethylamine → HCID 23440705, compound

https://huagongshe.com/reaction/2119339

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantPyBroPHCID 2733179—
ReactantHCID 9930132HCID 9930132—
ReactantPotassium tert-butoxideHCID 23665647—
SolventDimethylformamideHCID 6228—
SolventDichloromethane methanolHCID 21226129—
ProductHCID 23440705HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06686349B2
Source datasetuspto-grants-2004_02
ORD IDord-aeeb40cf30d04457899af43463d7c982
Source noteuspto-grants-2004_02