HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1665128Generated: November 1, 2026
4-(Aminomethyl)-1-(1-phenylethyl)piperidin-4-amine → HCID 178435989, compound
https://huagongshe.com/reaction/1665128
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-(Aminomethyl)-1-(1-phenylethyl)piperidin-4-amine | HCID 67086870 | — |
| Reactant | 3,5-Diamino-6-chloro-N-[(methylsulfanyl)methanimidoyl]pyrazine-2-carboxamide | HCID 140444318 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | HCID 178435989 | HCID 178435989 | — |
Reaction Steps
A mixture of 1-(3,5-diamino-6-chloro-pyrazine-2-carbonyl)-2-methyl-isothiourea (Intermediate A) (1.7 g, 4.54 mmol) and 4-aminomethyl-1-(1-phenyl-ethyl)-piperidin-4-ylamine (Intermediate BM) (1.6 g, 4.59 mmol) in propan-2-ol (50 ml) is stirred at 80° C. for 16 hours. The reaction mixture is concentrated in vacuo and purified by column chromatography (basic alumina, 0-2% MeOH in DCM) to obtain pale yellow solid. The compound obtained is further dissolved in MeOH and precipitated by adding diethyl ether. The supernatant solvent mixture is decanted and the product is washed again with diethyl ether and dried under vacuum to afford the title compound as off-white solid; [M+H]+ 429
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08039472B2 |
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| Source dataset | uspto-grants-2011_10 |
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| ORD ID | ord-a38cbe18d4064edeaa6b5d71f6624228 |
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| Source note | uspto-grants-2011_10 |
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