Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 852341Generated: October 30, 2026

Triethylamine → HCID 11618423, compound

https://huagongshe.com/reaction/852341

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant3,5-Difluorophenylacetic acidHCID 145424—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant2-Amino-pentanoic acid (5-tert-butyl-[1,3,4]thiadiazol-2-yl)-amideHCID 86033164—
SolventDichloromethaneHCID 6344—
ProductHCID 11618423HCID 11618423—

Reaction Steps

A mixture of 3,5-di-fluoro-phenyl acetic acid (51.6 mg, 0.3 mmol), 2-amino-pentanoic acid (5-tert-butyl-[1,3,4]thiadiazol-2-yl)-amide (88 mg, 0.3 mmol), HBOT (43 mg, 0.315 mmol), EDC HCl (69 mg, 0.36 mmol.) and triethylamine (0.17 ml) in methylene chloride was stirred at room temperature until product formation or disappearance of starting material. The mixture was quenched with water and extracted with methylene chloride. The organic layer was separated, washed with dilute HCl, brine, dried over sodium sulfate and the solvent was removed at reduced pressure to provide the title compound as a cude oil. The oil was purified by Shimadzu HPLC to provide the title compound as a white solid (56 mg), LC-MS M+1=411.2, 1H NMR(CDCL3) 8.7 (d, 1H,NH), 6.73(m,2H), 6.6(m, 1H), 4.7(m, 1H), 3.5(Abq, 2H), 1.6-1.9(m,2H), 1.3-1.6(m,2H), 1.5(s,9H), 0.92(t,3H) ppm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07253195B2
Source datasetuspto-grants-2007_08
ORD IDord-87d06ad5840b4d42b613fbbc7c0e9f48
Source noteuspto-grants-2007_08