HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2264371Generated: October 31, 2026
Ammonia → 5-[(4-Ethyl-1-piperazinyl)methyl]-2-pyridinamine
https://huagongshe.com/reaction/2264371
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ammonia | HCID 222 | — |
| Reactant | Piperazine, 1-[(6-broMo-3-pyridinyl)Methyl]-4-ethyl- | HCID 86642886 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 5-[(4-Ethyl-1-piperazinyl)methyl]-2-pyridinamine | HCID 45489910 | 54.5% |
Reaction Steps
Add liquid ammonia (50.0 kg) to a degassed mixture of 1-(6-bromo-pyridin-3-ylmethyl)-4-ethyl-piperazine (14.2 kg), cuprous oxide (200 g), and MeOH (57 kg) at T≦40° C. Heat the mixture at 65-75° C. overnight. Cool to 20-30° C. and filter over a Celite® pad. Concentrate the filtrate and add DCM (113 kg) and adjust the pH to 12-14 with sodium hydroxide 2N (23 kg) separate the phases and wash the organic phase with DCM (58×2 kg) and combine the organic layers. Filter the mixture through Celite® and concentrate. Dissolve the residue in toluene (9.7 kg) and crystallize by the addition of MtBE (8.3 kg) to give 6.0 kg of the title compound. Obtain further purification through a toluene recrystallization. MS (ES+): m/z=221 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07855211B2 |
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| Source dataset | uspto-grants-2010_12 |
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| ORD ID | ord-4e87e951fc5a4aa7a42029fa3c95d8cc |
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| Source note | uspto-grants-2010_12 |
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