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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1823326Generated: November 1, 2026

Triethylamine → HCID 11666673, compound

https://huagongshe.com/reaction/1823326

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantEthoxyacetyl chlorideHCID 84189—
ReactantHCID 11550312HCID 11550312—
SolventDichloromethaneHCID 6344—
ProductHCID 11666673HCID 1166667396%

Reaction Conditions

Temperature0 °C

Reaction Steps

A mixture of N7-(2-methylpropyl)-5-methyltetraazolo[1,5-a]pyridine-7,8-diamine (8.4 g, 38.1 mmol) in anhydrous dichloromethane (300 mL) was cooled to 0° C. under a nitrogen atmosphere, and triethylamine (5.3 mL, 38.1 mmol) was added. A solution of ethoxyacetyl chloride (4.7 g, 38.1 mmol) in dichloromethane (100 mL) was added dropwise over a period of five minutes, and a homogeneous solution resulted. After the solution was stirred for one hour, it was allowed to warm to room temperature, washed with water (2×200 mL), dried over magnesium sulfate, filtered, and concentrated under reduced pressure to provide 11.2 g of 2-ethoxy-N-{7-[(2-methylpropyl)amino]-5-methyltetraazolo[1,5-a]pyridin-8-yl}acetamide as a light tan solid, m.p. 182–185° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07038053B2
Source datasetuspto-grants-2006_05
ORD IDord-3f5b8958c44d4af0bfff85750cbb8691
Source noteuspto-grants-2006_05