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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1399962Generated: October 30, 2026

Ethyl isocyanate → 1-(5-Benzyloxy-7-bromo-benzothiazol-2-yl)-3-ethyl-urea

https://huagongshe.com/reaction/1399962

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl isocyanateHCID 8022—
Reactant5-(Benzyloxy)-7-bromobenzo[d]thiazol-2-amineHCID 57813588—
Solvent1,4-DioxaneHCID 31275—
Product1-(5-Benzyloxy-7-bromo-benzothiazol-2-yl)-3-ethyl-ureaHCID 5781362975.4%

Reaction Conditions

Temperature82.5 °C

Reaction Steps

To a suspension of vii (216 g, 0.64 mol) in 1,4-dioxane (4 L) was added ethylisocyanate (380 mL, 4.81 mol). The mixture was heated up to 80-85° C. overnight. The solvent was distilled off and the residue was co-evaporated with hexane. The residue was treated with H2O at 78-80° C. for 3-5 h. The resulting solid was filtered off and washed with hot H2O, dried under high vacuum to obtain viii (196 g, 75%). 1H-NMR (DMSO-d6, 400 MHz): δ 1.08 (t, J=7.20 Hz, 3H), 3.18 (q, J=6.80 Hz, 2H), 5.17 (s, 2H), 6.71 (br s, 1H), 7.15 (d, J=2.0 Hz, 1H), 7.26 (br s, 1H), 7.31-7.47 (m, 5H) and 10.82 (br s, 1H). MS: 405.90 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08906902B2
Source datasetuspto-grants-2014_12
ORD IDord-3445797094c04f1faf766d8767b17e2c
Source noteuspto-grants-2014_12