HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 624538Generated: October 31, 2026
Tetrahydrofuran → HCID 86711140, compound
https://huagongshe.com/reaction/624538
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 53780970 | HCID 53780970 | — |
| Reactant | tert-Butyl 3-(aminomethyl)-4-methylpiperazine-1-carboxylate | HCID 77474534 | — |
| Product | HCID 86711140 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09303041B2 |
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| Source dataset | uspto-grants-2016_04 |
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| ORD ID | ord-d81f86653bfe4a758c5427c5553cf9a5 |
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| Source note | uspto-grants-2016_04 |
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