Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 876794Generated: October 30, 2026

Water → 5-chlorothiazolo[5,4-b]pyridin-2-amine

https://huagongshe.com/reaction/876794

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantBromineHCID 24408—
Reactant5-Amino-2-chloropyridineHCID 79305—
ReactantPotassium thiocyanateHCID 516872—
SolventAcetic AcidHCID 176—
Product5-chlorothiazolo[5,4-b]pyridin-2-amineHCID 4266064—

Reaction Conditions

Temperature0 °C

Reaction Steps

To glacial acetic acid (125 mL) pre-cooled to 5° C. were added potassium thiocyanate (93 g, 961 mmol) and 6-chloropyridin-3-amine (Q-1) (15 g, 117 mmol). The mixture was placed in a freezing mixture of ice and salt and stirred, while 10 mL of bromine in glacial acetic acid (30 mL) was added from an addition funnel at such a rate that the temperature never rose beyond 0° C. After all the bromine had been added, the solution was stirred for an additional 2 h at 0° C. and at room temperature overnight. Water (60 mL) was added quickly, and the slurry maintained at 90° C. was filtered hot. The orange filter cake was placed in the reaction flask. Glacial acetic acid (60 mL) was added to the flask. The mixture in the flask was maintained at 85° C. was filtered hot once again. The combined filtrates were cooled and neutralized with concentrated ammonia solution to pH 6. A precipitate was collected as the title compound (19 g). MS (m/z): 186 (M+1)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08987269B2
Source datasetuspto-grants-2015_03
ORD IDord-5641ada09b4f49b5bc12f35b4c517f37
Source noteuspto-grants-2015_03