HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2287157Generated: October 31, 2026
Piperazine → 2-(1-Piperazinyl)-4,6-bis[(1,1,2,2-tetramethylpropyl)amino]-s-triazine
https://huagongshe.com/reaction/2287157
Participants
| Role | Name | HCID | Charge |
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| Reactant | Piperazine | HCID 4837 | — |
| Reactant | 2-Chloro-4,6-di(2,3,3-trimethyl-2-butyl)amino-s-triazine | HCID 15572577 | — |
| Solvent | 2-Methoxyethanol | HCID 8019 | — |
| Product | 2-(1-Piperazinyl)-4,6-bis[(1,1,2,2-tetramethylpropyl)amino]-s-triazine | HCID 23459503 | — |
Reaction Steps
A 21 g. portion of piperazine in 500 ml. of methyl cellosolve is treated with 17.1 g. of 2-chloro-4,6-bis[(1,1,2,2-tetramethylpropyl)amino]-s-triazine. The mixture is stirred at reflux for 8 hours and then at room temperature. The mixture is filtered and the filtrate is taken to dryness in vacuo. The residue is shaken with 200 ml. of water, filtered, the insolubles collected, washed with 500 ml. of water and dried. The solid is suspended in 500 ml. of boiling ethanol, 150 ml. of methyl cellosolve is added and the mixture is concentrated to 300 ml., clarified and cooled to 10° C. The mixture is then taken to dryness in vacuo and the residue is recrystallized from 250 ml. of 60% ethanol with charcoal. The solid is washed with 100 ml. of 50% cold ethanol and dried giving the desired product, m.p. 183°-185° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04269832 |
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| Source dataset | uspto-grants-1981_05 |
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| ORD ID | ord-9de76110a28d46b58057233775d435c8 |
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| Source note | uspto-grants-1981_05 |
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