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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1966251Generated: October 31, 2026

Ammonium Hydroxide → [3-(2-Methoxy-ethoxy)-5-(pyridine-3-yloxy)-pyridine-2-yl]-thiourea

https://huagongshe.com/reaction/1966251

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium HydroxideHCID 14923—
Reactant1,1'-ThiocarbonyldiimidazoleHCID 80264—
Reactant3-(2-Methoxy-ethoxy)-5-(pyridine-3-yloxy)-pyridine-2-ylamineHCID 67486505—
SolventTetrahydrofuranHCID 8028—
Product[3-(2-Methoxy-ethoxy)-5-(pyridine-3-yloxy)-pyridine-2-yl]-thioureaHCID 8664460969%

Reaction Steps

3-(2-Methoxy-ethoxy)-5-(pyridine-3-yloxy)-pyridine-2-ylamine (0.48 mmol) is dissolved in THF (7 ml) and 1,1′-thiocarbonyldiimidazole (4 eq.) is added. The reaction solution is stirred 2 days. 32% NH4OH (20 eq.) is added and stirred 4 hours at room temperature. The solved is removed in vacuo and water (150 ml) is added and extracted with dichloromethane. The combined organic layers are washed with brine and dried over MgSO4. The solvent is removed in vacuo. [3-(2-Methoxy-ethoxy)-5-(pyridine-3-yloxy)-pyridine-2-yl]-thiourea is obtained as yellow solid in a yield of 69%. HPLC (method C): 1.15 min; LC-MS (method A): 0.9 min, 321.15 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08420642B2
Source datasetuspto-grants-2013_04
ORD IDord-51cb5a33446f4ade8eddea750ff1bbd2
Source noteuspto-grants-2013_04