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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1748249Generated: October 29, 2026

Trifluoroacetic acid → ethyl (4R)-4-methyl-1-oxo-1,2,3,4-tetrahydropyrazino[1,2-a]indole-7-carboxylate

https://huagongshe.com/reaction/1748249

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantPotassium CarbonateHCID 11430—
Reactantdiethyl 1-{(2R)-1-[(tert-butoxycarbonyl)amino]propan-2-yl}-1H-indole-2,6-dicarboxylateHCID 67235704—
SolventEthanolHCID 702—
SolventDichloromethaneHCID 6344—
Productethyl (4R)-4-methyl-1-oxo-1,2,3,4-tetrahydropyrazino[1,2-a]indole-7-carboxylateHCID 6723547074.6%

Reaction Steps

To a solution of diethyl 1-{(2R)-1-[(tert-butoxycarbonyl)amino]propan-2-yl}-1H-indole-2,6-dicarboxylate (2.7 g, 6.4 mmol) in CH2Cl2 (10 mL) is added TFA (10 mL). The reaction mixture is stirred for 2 h and the solvent is removed under vacuum. To a solution of the residue in ethanol (30 mL) is added K2CO3 (4.5 g, 32.3 mmol) and the reaction mixture is stirred at room temperature for 16 h. The solvent is evaporated and the residue is taken up in water. To the mixture is added a small amount of diethyl ether followed by heptanes (100 mL). The suspension is filtered to afford the title compound (1.3 g, 57% for two steps) as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09150577B2
Source datasetuspto-grants-2015_10
ORD IDord-3f79631ac7064fad8aefb992a4a8ebfa
Source noteuspto-grants-2015_10