HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1943013Generated: October 26, 2026
Sodium Sulfate → 1-[3-(4-Methylpiperazin-1-yl)-2,3,4,5-tetrahydrooxepin-3-yl]methanamine
https://huagongshe.com/reaction/1943013
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Sulfate | HCID 24436 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Reactant | Ethyl 4-(3-cyano-2,3,4,5-tetrahydrooxepin-3-yl)piperazine-1-carboxylate | HCID 58415949 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-[3-(4-Methylpiperazin-1-yl)-2,3,4,5-tetrahydrooxepin-3-yl]methanamine | HCID 58415926 | 97% |
Reaction Steps
To a solution of ethyl 4-(3-cyano-2,3,4,5-tetrahydrooxepin-3-yl)piperazine-1-carboxylate (320 mg, 1.146 mmole) in dry THF (5 ml) was added LAH (1.75 ml, 3.50 mmole) at 0° C. After 30 min the mixture was warmed to RT. After 16 hr the mixture was cooled to 0° C. and slowly quenched with 2M NaOH until gas evolution had ceased and a fine white precipitate formed. Anhydrous Na2SO4 was added and the mixture stirred for 15 min. The slurry was filtered through a pad of Celite washing with THF. The filtrate was concentrated to give the title compound as a clear oil (250 mg, 97%) which was used in the next step without purification. 1H-NMR (CDCl3, 500 MHz) d 6.23 (d, J=6.83 Hz, 1 H), 4.60 (m, 1 H), 4.11 (dd AB, J=12.46 and 58.83 Hz, 2 H), 2.77 (s, 2 H), 2.70 (m, 4 H), 2.43 (m, 4 H), 2.27 (s, 3 H), 2.13 (m, 4 H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08389720B2 |
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| Source dataset | uspto-grants-2013_03 |
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| ORD ID | ord-385f46438cac4c24a644b42e00c74b5a |
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| Source note | uspto-grants-2013_03 |
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