HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 651348Generated: October 26, 2026
Diisopropylethylamine → N-(5-(8-Naphthalen-1-ylmethyl-4-oxo-1-phenyl-1,3,8,-triazaspiro[-4.5]dec-3-yl)pentyl)guanidine
https://huagongshe.com/reaction/651348
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 3,5-Dimethyl-1H-pyrazole-1-carboxamidine mononitrate | HCID 198186 | — |
| Reactant | 3-(5-Aminopentyl)-8-naphthalen-1-ylmethyl-1-phenyl-1,3,8-triaza-spiro[4.5]decan-4-one | HCID 20679434 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | N-(5-(8-Naphthalen-1-ylmethyl-4-oxo-1-phenyl-1,3,8,-triazaspiro[-4.5]dec-3-yl)pentyl)guanidine | HCID 178512825 | 5.2% |
Reaction Steps
3-(5-Aminopentyl)-8-naphthalen-1-ylmethyl-1-phenyl-1,3,8-triaza-spiro[4.5]decan-4-one, di-trifluoroacetate (0.137 g, 0.2 mmol) prepared as described in Example 13, was dissolved in dimethylformamide (1 ml) and diisopropylethylamine (0.233 g, 1.8 mmol) and 3,5-dimethylpyrazol-1-carboxamidine nitrate (0.060 g, 0.3 mmol) was added. The mixture was stirred at room temperature for 1 h and the addition of an equal amount 3,5-dimethylpyrazol-1 carboxamidine nitrate was repeated. After stirring for 16 h the mixture was diluted with water (10 ml) and extracted with ether (5×10 ml). The aqueous phase and undissolved syrup were extracted with dichloromethane (10 ml), the dichloromethane solution was washed with water (5×10 ml), dried over MgSO4 and concentrated in vacuo, affording the title compound (0.047 g, 5.2%) as an amorphous powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06277991B1 |
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| Source dataset | uspto-grants-2001_08 |
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| ORD ID | ord-8e43e02b6f0b472cbbea7341b6042c53 |
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| Source note | uspto-grants-2001_08 |
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