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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 624538Generated: October 31, 2026

Tetrahydrofuran → HCID 86711140, compound

https://huagongshe.com/reaction/624538

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 53780970HCID 53780970—
Reactanttert-Butyl 3-(aminomethyl)-4-methylpiperazine-1-carboxylateHCID 77474534—
ProductHCID 86711140HCID 86711140—

Reaction Steps

To a mixture of tert-butyl 3-(aminomethyl)-4-methylpiperazine-1-carboxylate, prepared as described in the previous step, (5.5 g, crude) and sodium bicarbonate (2.52 g, 30 mmol) in tetrahydrofuran (100 mL) was added a solution of 2H-isoindole-2-carboxylic acid, 1,3-dihydro-1,3-dioxo-, ethyl ester (6.59 g, 30 mmol) in tetrahydrofuran (20 mL) at ambient temperature. After stirring for 30 minutes, the suspension was filtered, and the filtrate was concentrated to give crude product which was purified by column chromatography to provide the title compound. 1H NMR (400 MHz, MeOD) δ 7.87-7.85 (m, 2H), 7.87-7.80 (m, 2H), 3.94-3.90 (m, 1H), 3.75-3.65 (br, 3H), 3.43-3.41 (br, 1H), 3.30-3.28 (m, 2H), 3.49 (s, 3H), 2.39-2.38 (m, 1H), 2.30-2.28 (m, 1H), 1.36 (s, 9H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09303041B2
Source datasetuspto-grants-2016_04
ORD IDord-d81f86653bfe4a758c5427c5553cf9a5
Source noteuspto-grants-2016_04