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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 895979Generated: October 30, 2026

Iodoethane → 2-Ethyl-1-(11-oxo-10,11-dihydro-5H-dibenzo[b,e][1,4]diazepin-2-yl)-isothiourea

https://huagongshe.com/reaction/895979

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodoethaneHCID 6340—
Reactant(11-Oxo-10,11-dihydro-5H-dibenzo[b,e][1,4]diazepin-2-yl)-thioureaHCID 11300593—
SolventDimethyl SulfoxideHCID 679—
Product2-Ethyl-1-(11-oxo-10,11-dihydro-5H-dibenzo[b,e][1,4]diazepin-2-yl)-isothioureaHCID 17847746399.7%

Reaction Steps

To a solution of (11-oxo-10,11-dihydro-5H-dibenzo[b,e][1,4]diazepin-2-yl)-thiourea (Example 9, 100 mg, 0.35 mmol) in DMSO was added ethyl iodide (28.2 μL, 0.35 mmol). The mixture was stirred at room temperature for 48 hr. DMSO was removed under vacuum and the residue was partitioned between ethyl acetate and saturated aqueous sodium bicarbonate. The organic layer was dried with magnesium sulfate, filtered and the solvent evaporated to give a yellow semi-solid which was chromatographed on silica gel (10% methanol/90% ethyl acetate) to give a yellow solid (109 mg, 55%). H1 NMR (DMSO d6) δ: 8.96 (s, 1H), 7.34 (s, 1H), 7.09-7.03 (m, 2H), 6.99-6.93 (m, 4H), 6.88-6.86 (m, 3H), 3.0-2.95 (q, 1H, J=7), 1.30-1.27 (t, 3H, J=7), MS (ES): MH+ 313.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06919328B1
Source datasetuspto-grants-2005_07
ORD IDord-ccfaa2002b6a404d97fcd3340a9691ad
Source noteuspto-grants-2005_07