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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 911062Generated: October 31, 2026

Benzoyl isothiocyanate → 1-Benzoyl-3-(4-(benzyloxy)-5-bromopyridin-2-yl)thiourea

https://huagongshe.com/reaction/911062

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl isothiocyanateHCID 68284—
ReactantHCID 66618159HCID 66618159—
SolventTetrahydrofuranHCID 8028—
Product1-Benzoyl-3-(4-(benzyloxy)-5-bromopyridin-2-yl)thioureaHCID 8663477591.5%

Reaction Steps

A flask was charged with 4-(benzyloxy)-5-bromopyridin-2-amine (6.90 g, 24.7 mmol), and THF (250 mL). Benzoyl isothiocyanate (4.24 g, 26.0 mmol) was added and the reaction was stirred at ambient temperature overnight. The reaction mixture was concentrated, and 9:1 Hexanes:ethyl acetate (400 mL) was added to the residue. The suspension was filtered to give the desired product (10 g, 82.3% yield) as light brown solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08022222B2
Source datasetuspto-grants-2011_09
ORD IDord-baede6bb2c7b4824a17ca99cfc25060e
Source noteuspto-grants-2011_09