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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 415650Generated: October 29, 2026

Boron tribromide → 5-Bromo-2-bromomethyl-thiazolo[5,4-b]pyridine

https://huagongshe.com/reaction/415650

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron tribromideHCID 25134—
Reactant2-Benzyloxymethyl-5-bromo-thiazolo[5,4-b]pyridineHCID 86643276—
SolventSodium BicarbonateHCID 516892—
Product5-Bromo-2-bromomethyl-thiazolo[5,4-b]pyridineHCID 86643275136.1%

Reaction Conditions

Temperature25 °C

Reaction Steps

A solution of 2-Benzyloxymethyl-5-bromo-thiazolo[5,4-b]pyridine (1.60 g, 4.77 mmol) DCM (15 mL) was cooled to −78° C. followed by addition of BBr3 (2.27 ml, 23.86 mmol). The reaction mixture was stirred at 25° C. for 2 h. After the completion of the reaction mixture (TLC monitoring), solution of NaHCO3 (20 mL) was added at 0° C. and extracted with ethyl acetate (3×50 mL). The combined organics was washed with water, brine, dried (Na2SO4), filtered and concentrated to get the desired product (2.0 g, Crude yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08088791B2
Source datasetuspto-grants-2012_01
ORD IDord-cfeb28efa7414b6197e9f243bb1339a4
Source noteuspto-grants-2012_01