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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 705101Generated: October 31, 2026

1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide → HCID 46830534, compound

https://huagongshe.com/reaction/705101

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantCarbodiimideHCID 160435—
Reactant2-(Aminomethyl)-5-methylpyrazineHCID 2756496—
ReactantHCID 59370290HCID 59370290—
SolventDichloromethaneHCID 6344—
SolventTriethylamineHCID 8471—
ProductHCID 46830534HCID 46830534—

Reaction Steps

3-(4-Isopropyl-[1,2,3]thiadiazol-5-yl)-N-(5-methyl-pyrazin-2-ylmethyl)-5-(5-methyl-pyridin-2-yl)-benzamide was prepared using the carbodiimide-based amide synthesis procedure of example 7 in published patent application US2008004442. Briefly, 3-(4-isopropyl-[1,2,3]thiadiazol-5-yl)-5-(5-methyl-pyridin-2-yl)-benzoic acid, C-(5-methyl-pyrazin-2-yl)-methylamine, EDCI, HOBt and Et3N were added to methylene chloride, and the mixture was stirred at room temperature for 16 hours, then was partitioned between water and methylene chloride. The combined organic layers were dried (MgSO4), filtered and concentrated under reduced pressure. The resulting residue was purified via flash chromatography to give3-(4-isopropyl-[1,2,3]thiadiazol-5-yl)-N-(5-methyl-pyrazin-2-ylmethyl)-5-(5-methyl-pyridin-2-yl)-benzamide, MS (M+H)=445.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09173861B2
Source datasetuspto-grants-2015_11
ORD IDord-df0dcaf65bdc4ecc88330166ac4652b9
Source noteuspto-grants-2015_11