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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 255084Generated: October 31, 2026

1-Adamantanecarboxylic acid → HCID 178472637, compound

https://huagongshe.com/reaction/255084

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Adamantanecarboxylic acidHCID 13235—
ReactantDiisopropylethylamineHCID 81531—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
ReactantHCID 131728626HCID 131728626—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductHCID 178472637HCID 17847263781%

Reaction Conditions

Temperature65 °C

Reaction Steps

To a solution of the product from Example 77A (0.75 g, 2.8 mmol) and 1-adamantanecarboxylic acid (0.56 g, 3.1 mmol) in 14 mL of THF at 0° C. was added O-(7-azabenzotriazol-1-yl)-N,N,N′,N′-tetramethyluronium hexafluorophosphate (12 g, 3.1 mmol) and diisopropylethylamine (1.1 mL, 6.2 mmol). The mixture was heated to 65° C. for 2.5 hours, cooled to ambient temperature and then diluted with ethyl acetate. The mixture was washed twice with water, saturated aqueous sodium bicarbonate, and brine. The organic extract was dried over magnesium sulfate, and concentrated under reduced pressure. Purification by column chromatography (SiO2, 30-50% ethyl acetate/hexanes gradient) afforded 0.79 g (81%) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07875639B2
Source datasetuspto-grants-2011_01
ORD IDord-d2d329845e874d56a03061827a2c20bd
Source noteuspto-grants-2011_01