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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2210819Generated: November 2, 2026

Ethyl Acetate → 3-(1,2,3,4,10,14b-Hexahydrodibenzo[c,f]pyrazino[1,2,a]azepin-2-yl)propyl carbamate

https://huagongshe.com/reaction/2210819

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantTrichloroacetyl isocyanateHCID 76400—
ReactantHCID 18999734HCID 18999734—
SolventDichloromethaneHCID 6344—
Product3-(1,2,3,4,10,14b-Hexahydrodibenzo[c,f]pyrazino[1,2,a]azepin-2-yl)propyl carbamateHCID 1899971959%

Reaction Steps

0.2 ml of trichloroacetyl isocyanate were added to a solution of 400 mg of 3-(1,2,3,4,10,14b-hexahydrodibenzo[c,f]pyrazino[1,2-a]azepin-2-yl)propanol (prepared as described in Example 16) in 20 ml of methylene chloride, whilst ice-cooling, and the mixture was stirred at room temperature for 2 hours. At the end of this time, the solvent was removed by distillation under reduced pressure. The resulting residue was dissolved in 22 ml of methanol, 9.0 g of silica gel were added to the solution and the mixture was stirred at room temperature for 15 hours. At the end of this time, the mixture was filtered using a Celite (trade mark) filter aid, and the filtrate was concentrated by evaporation under reduced rates pressure. The residue was subjected to column chromatography through silica gel eluted with ethyl acetate, to give, after recrystallization from ethyl acetate, 260 mg (yield 59%) of the title compound as crystals, melting at 160°-151° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05461051
Source datasetuspto-grants-1995_10
ORD IDord-d85ae8fc8e8a465c868d89b35ccea6be
Source noteuspto-grants-1995_10