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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1433179Generated: November 3, 2026

Ethyl 2-chloroethanecarboximidate hydrochloride → HCID 178449971, compound

https://huagongshe.com/reaction/1433179

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 2-chloroethanecarboximidate hydrochlorideHCID 12470659—
Reactant3',4'-Diamino-biphenyl-2-sulfonic acid tert-butylamideHCID 57934964—
SolventEthanolHCID 702—
ProductHCID 178449971HCID 17844997160%

Reaction Steps

A mixture of 3′,4′-diamino-biphenyl-2-sulfonic acid tert-butylamide (1.0 g, 3.13 mmol), 2-chloroacetimidic acid ethyl ester hydrochloride salt (591 mg, 3.76 mmol) (prepared according to the procedure described in J. Med. Chem., 1986, 29, 2280) in anhydrous ethanol (100%, 20 mL) was stirred at room temperature for 4 h. The reaction mixture was concentrated under reduced pressure and extracted with ethyl acetate and brine. The organic layer was dried over Na2SO4, filtered, and the filtrate was concentrated in vacuo. The residue was purified by chromatography (silica, EtOAc) to afford the title compound as an off-white solid (708 mg, 60% yield). 1H NMR (400 MHz, CD3OD) δ (ppm): 8.14 (dd, 1H, J=8.1 Hz, J=1.5 Hz), 7.79 (m, 1H), 7.74 (dd, 1H, J=8.5 Hz, J=1.1 Hz), 7.65 (td, 1H, J=7.5 Hz, J=1.6 Hz), 7.57 (td, 1H, J=7.8 Hz, J=1.6 Hz), 7.50 (dd, 1H, J=8.3 Hz, J=1.6 Hz), 7.39 (dd, 1H, J=7.3 Hz, J=1.2 Hz), 5.05 (s, 2H), 1.02 (s, 9H). Mass Spectrum (LCMS, ESI pos.) Calcd. For C18H20ClN3O2S: 378.89 (M+H), Found 378.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07612211B2
Source datasetuspto-grants-2009_11
ORD IDord-4b8f14e65fd547ab9459ef146c649d1f
Source noteuspto-grants-2009_11