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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 415842Generated: October 31, 2026

Triethylamine → HCID 178505125, compound

https://huagongshe.com/reaction/415842

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant(Z)-4-amino-N-hydroxy-1,2,5-oxadiazole-3-carbonimidoyl chlorideHCID 4040027—
ReactantN-(2-Aminoethyl)methanesulfonamide dihydrochlorideHCID 86638021—
SolventEthanolHCID 702—
ProductHCID 178505125HCID 178505125100.9%

Reaction Conditions

Temperature0 °C

Reaction Steps

4-Amino-N-hydroxy-1,2,5-oxadiazole-3-carboximidoyl chloride (9.7 g, 60 mmol) was stirred in ethanol (460 mL) and N-(2-aminoethyl)methanesulfonamide dihydrochloride (19 g, 109 mmol) was added slowly in portions and the temperature rose to 25° C. After cooling back to 0° C., triethylamine (53 mL, 380 mmol) was added dropwise over 15 minutes and the reaction was stirred for an additional 15 minutes. The solution was washed with water (300 mL) and brine (300 mL). The organic layer was dried over sodium sulfate and concentrated in vacuo to give the desired product (16 g, 100%). LCMS calculated for C6H13N6O4S (M+H)+: m/z=265.1. 1H NMR (400 MHz, DMSO-d6): δ 10.16 (s, 1H), 9.07 (m, 1H), 7.18 (m, 1H), 6.37 (s, 2H), 3.36 (m, 2H), 3.15 (m, 2H), 2.87 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08088803B2
Source datasetuspto-grants-2012_01
ORD IDord-57daa41c5a3f434180d725f6b2ae4123
Source noteuspto-grants-2012_01