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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1183813Generated: October 30, 2026

Trifluoroacetic acid → 6-tert-butyl 2-methyl 7,8-dihydropyrrolo[3,2-e]indole-2,6(3H)-dicarboxylate

https://huagongshe.com/reaction/1183813

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantPiperidineHCID 8082—
ReactantMethyl 3,6,7,8-tetrahydropyrrolo[3,2-e]indole-2-carboxylateHCID 15480266—
ReactantHCID 178496869HCID 178496869—
SolventDimethylformamideHCID 6228—
SolventDiisopropylethylamineHCID 81531—
Product6-tert-butyl 2-methyl 7,8-dihydropyrrolo[3,2-e]indole-2,6(3H)-dicarboxylateHCID 15114773—

Reaction Conditions

Temperature25 °C

Reaction Steps

A solution of 3 (15 mg, 0.014 mmol) in DMF (2 mL) was treated with 5% piperidine in DMF (2 mL) and the reaction mixture was stirred for 10 min at 25° C. The crude product was precipitated with diethyl ether and used for the next step without further purification. The crude product was dissolved in DMF (3 mL) followed by the addition of 4 (25 mg, 0.025 mmol) in DMF (2 mL) and DIEA (20 uL). The reaction mixture was stirred for 2 hrs at room temperature. TFA was added to the reaction mixture and the reaction mixture was stirred at room temperature for 45 min to yield compound 5 as indicated by analytical HPLC. Crude product was purified by Prep HPLC (SymmetrPrep C18, 7 μm, 19×150 mm column), eluted at 10 ml/min (0.01% TFA in water/acetonitrile) with a gradient: 10% acetonitrile in 5 min, 10% to 50% acetonitrile in 15 min, maintaining 50% acetonitrile in 5 min, 50% to 100% acetonitrile in 5 min, to obtain 5 (3 mg, 94%). MS: (MH)+ 889.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08664407B2
Source datasetuspto-grants-2014_03
ORD IDord-440b70ca10bb44bf8a49318adf694142
Source noteuspto-grants-2014_03