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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1506164Generated: November 1, 2026

Ammonium Chloride → HCID 86726617, compound

https://huagongshe.com/reaction/1506164

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantMethanamine, N-methoxy-, hydrochloride (1:1)HCID 81138—
ReactantDiisopropylethylamineHCID 81531—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant3-Hydroxyadamantane-1-carboxylic acidHCID 2736518—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
ProductHCID 86726617HCID 86726617135.5%

Reaction Conditions

Temperature40 °C

Reaction Steps

3-Hydroxyadamantane-1-carboxylic acid (500 mg, 2.55 mmol) in dichloromethane (15 mL) was mixed with 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (587 mg, 3.06 mmol), 1-hydroxybenzotriazole (103 mg, 0.765 mmol), N,O-dimethylhydroxylamine hydrochloride (298 mg, 3.06 mmol) and N,N-diisopropylethylamine (1.06 mL, 6.12 mmol) and then stirred at 40° C. for 2 hours. The reaction mixture was stirred with 4-dimethylaminopyridine (779 mg, 6.38 mmol) at 40° C. for 2 hours. After addition of saturated aqueous ammonium chloride, the reaction mixture was extracted with chloroform. The organic layer was washed with 1M hydrochloric acid and saturated aqueous sodium chloride, dried over anhydrous sodium sulfate and concentrated under reduced pressure to give the title compound as a yellow oil (248 mg, yield 41%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09216999B2
Source datasetuspto-grants-2015_12
ORD IDord-ed72f1912b244b4ca6dfb040d8ac4ace
Source noteuspto-grants-2015_12