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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1948709Generated: October 26, 2026

2-Aminoadamantane → HCID 66884685, compound

https://huagongshe.com/reaction/1948709

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-AminoadamantaneHCID 25332—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
ReactantDiisopropylethylamineHCID 81531—
Reactant1,7-Diaza-spiro(4.4)nonane-1-carboxylic acid tert-butyl esterHCID 42614573—
SolventDichloromethaneHCID 6344—
ProductHCID 66884685HCID 6688468589%

Reaction Steps

A solution of adamantan-2-ylamine (75 mg, 0.38 mmol), CDI (80 mg, 0.46 mmol), i-Pr2NEt (150 mg, 1.14 mmol) in CH2Cl2 (5 mL) was stirred at 0° C. for 1 h, and tert-butyl 1,7-diazaspiro[4.4]nonane-1-carboxylate (100 mg, 0.38 mmol) was added. The reaction mixture stirred at room temperature overnight. The solvent was removed under reduced pressure to give crude product which was purified by preparative TLC to afford tert-butyl 7-(2-adamantylcarbamoyl)-1,7-diazaspiro[4.4]nonane-1-carboxylate (136 mg, 89%). LC-MS Method 3, tR=4.24 min, m/z=404.1; 1H NMR (CDCl3) 1.39 (s, 9H), 1.48-1.52 (m, 4H), 1.62-1.71 (m, 5H), 1.71-1.81 (m, 10H), 1.81-1.88 (m, 3H), 1.89-2.01 (m, 1H), 2.93-3.12 (m, 1H), 3.21 (m, 1H), 3.28-3.49 (m, 2H), 3.55 (m, 1H), 3.68 (m, 1H), 3.88 (m, 1H), 4.46 (m, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08399504B2
Source datasetuspto-grants-2013_03
ORD IDord-9337fdb47887490ab580e585fca1c008
Source noteuspto-grants-2013_03