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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1049089Generated: November 1, 2026

Triethylamine → Ethyl 4-{1-[(adamantan-1-ylcarbonyl)amino]-2-methylpropyl}benzoate

https://huagongshe.com/reaction/1049089

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant1-Adamantanecarboxylic acidHCID 13235—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
ReactantEthyl 4-(1-amino-2-methylpropyl)benzoateHCID 58417523—
SolventDimethylformamideHCID 6228—
ProductEthyl 4-{1-[(adamantan-1-ylcarbonyl)amino]-2-methylpropyl}benzoateHCID 67396119—

Reaction Steps

To a vial charged with 1-adamantylcarboxylic acid (0.031 g, 0.17 mmol) was added HATU (64.6 mg, 0.17 mmol), triethylamine (0.14 mL, 1.02 mmol) and DMF (1 mL). The solution was shaken at rt for 1 h then ethyl 4-(1-amino-2-methylpropyl)benzoate (0.038 g, 0.17 mmol) in DMF (1 mL) was added. The resulting mixture was shaken at rt for 16 h. Solvent was then evaporated. To the residue was added DCE (3 mL) and sat. NaHCO3 solution (1.5 mL). After separation, the aqueous layer was extracted with DCE twice. Combined organic layers were concentrated to give crude ethyl 4-{1-[(adamantan-1-ylcarbonyl)amino]-2-methylpropyl}benzoate as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09382197B2
Source datasetuspto-grants-2016_07
ORD IDord-2645a3bf51694e8abbe29dba18e9ee51
Source noteuspto-grants-2016_07