HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 18406Generated: October 30, 2026
2-(Adamantan-1-yl)-N-methylethan-1-amine → HCID 21974209, compound
https://huagongshe.com/reaction/18406
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-(Adamantan-1-yl)-N-methylethan-1-amine | HCID 35996 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Triphosgene | HCID 94429 | — |
| Reactant | N-Methyl-3-(pyridin-4-yl)propan-1-amine | HCID 21974070 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 21974209 | HCID 21974209 | 141.6% |
Reaction Steps
A solution of triphosgene (190 mg, 0.640 mmol) in dichloromethane (6.0 ml) was stirred at room temperature under a nitrogen atmosphere. A solution of 2-(1-adamantyl)-N-methylethylamine (Intermediate No. 3-1, 330 mg, 1.71 mmol) and diisopropylethylamine (0.357 ml, 2.05 mmol) in dichloromethane (6.0 ml) was added dropwise thereto over 17 minutes. After eight minutes, a solution of N-methyl-3-(4-pyridyl)propylamine (Intermediate No. 3-3, 264 mg, 1.78 mmol) and diisopropylethylamine (0.357 ml, 2.05 mmol) in dichloromethane (5.1 ml) was added to the mixture all at once, and the whole was stirred for 20 hours. The reaction mixture was diluted with diethyl ether (40 ml), the whole was washed with a saturated aqueous sodium hydrogencarbonate solution (40 ml) twice and a saturated aqueous sodium chloride solution (40 ml) successively, and the organic layer was dried over magnesium sulfate. The solvent was evaporated under reduced pressure, and the residue was purified by silica gel column chromatography to give the target compound (335 mg, 54%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07741346B2 |
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| Source dataset | uspto-grants-2010_06 |
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| ORD ID | ord-cd3da273f43049dbbedd26fabce8ed1e |
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| Source note | uspto-grants-2010_06 |
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