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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1582573Generated: October 31, 2026

Hydrochloric Acid → HCID 22718141, compound

https://huagongshe.com/reaction/1582573

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTriethylamineHCID 8471—
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantRac-(1r,4r)-4-methoxycyclohexane-1-carboxylic acidHCID 736153—
Reactant2,3-DiaminobenzamideHCID 10487029—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 22718141HCID 2271814164%

Reaction Steps

1.4 g (8.9 mmol) of 4-methoxycyclohexanecarboxylic acid were dissolved in 30 ml of tetrahydrofuran and, at 0° C., successively 1.9 g (1.8 mmol) of N′-(3-dimethylaminopropyl)-N-ethylcarbodiimide×hydrochloride, 1.8 g (11.6 mmol) of N-hydroxybenzotriazole and 1.95 g (19.2 mmol) of triethylamine were added. The mixture was stirred for 1 hour. Then 2.0 g (8.9 mmol) of 2,3-diaminobenzamide×2 hydrochloride and 1.95 g (19.2 mmol) of triethylamine were added. The mixture was then stirred at 0° C. for 1 hour and at room temperature for 16 hours. The mixture was diluted with a large amount of water and extracted several times with ethyl acetate. The organic phases were combined, dried and concentrated in vacuo. 1.5 g of the product were obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06737421B1
Source datasetuspto-grants-2004_05
ORD IDord-ae7aaf71cf974d31b4f7d7c10e9f979d
Source noteuspto-grants-2004_05