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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 44446Generated: October 28, 2026

Cyclohexylamine → HCID 136169029, compound

https://huagongshe.com/reaction/44446

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclohexylamineHCID 7965—
ReactantTriethylamineHCID 8471—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant1293289-69-6HCID 136008904—
ReactantHCID 178418300HCID 178418300—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
ProductHCID 136169029HCID 13616902971.7%

Reaction Steps

To the stirred suspension of [(2-hydroxy-4-oxo-6,7,8,9-tetrahydro-4H,5H-10-thia-1,4a-diaza-benzo[a]azulene-3-carbonyl)-amino]-acetic acid (0.70 gm, 0.0020 mole) in dichloromethane (20 ml), triethylamine (0.85 ml, 0.0062 mole) and cyclohexylamine (0.29 ml, 0.0025 mole) were added. To the reaction mixture, hydroxybenzotriazole (0.28 gm, 0.0020 mole) and 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (0.60 gm, 0.0031 mole) were added and stirred at room temperature for 12 hrs. Dichloromethane was distilled off and 1N hydrochloric acid (50 ml) was added to the residue, the separated solid was collected by filtration. The solid thus obtained was stirred in methanol (20 ml) at 60° C. for 0.5 hr, filtered and suck dried to give 0.60 gm title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08541430B2
Source datasetuspto-grants-2013_09
ORD IDord-53ad18cf92a6496c8e32d1d38f5ee661
Source noteuspto-grants-2013_09