HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 443763Generated: October 27, 2026
Acetone → 3-[4-Chloro-6-(1,1,3,3-tetramethylbutylamino)-s-triazin-2-yl]-3-azabicyclo[3.2.2]nonane
https://huagongshe.com/reaction/443763
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetone | HCID 180 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | tert-Octylamine | HCID 61017 | — |
| Reactant | 3-(4,6-Dichloro-s-triazin-2-yl)-3-azabicyclo[3.2.2]nonane | HCID 15572579 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3-[4-Chloro-6-(1,1,3,3-tetramethylbutylamino)-s-triazin-2-yl]-3-azabicyclo[3.2.2]nonane | HCID 15572580 | — |
Reaction Steps
Thirty grams (0.11 mole) of 3-(4,6-dichloro-s-triazin-2-yl)-3-azabicyclo[3.2.2]nonane is dissolved in 300 ml. of acetone and then 370 ml. of water is added followed by 20 g. (0.15 mole) of tert-octylamine. After stirring for 10 minutes, 4.4 g. (0.11 mole) of NaOH in 30 ml. of water is added over 20 minutes. The reaction is then heated to reflux for 19 hours. After cooling to room temperature, one liter of water is added, stirred for one hour and the white precipitate filtered off. The precipitate is washed with water, dried overnight, dissolved in dichloromethane and filtered through Magnesol®. The Magnesol® is then washed with dichloromethane, solvent removed in vacuo and recrystallized from dichloromethane-hexanes giving 20 g. of colorless crystals, m.p. 159°-162.5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04261892 |
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| Source dataset | uspto-grants-1981_04 |
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| ORD ID | ord-66194526f06b4de2bcb4624a4b33bb40 |
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| Source note | uspto-grants-1981_04 |
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