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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 335502Generated: October 29, 2026

Potassium Bromide → CID 71271091

https://huagongshe.com/reaction/335502

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium BromideHCID 253877—
ReactantTempoHCID 2724126—
ReactantSodium HypochloriteHCID 23665760—
ReactantThiamet G, >=98% (HPLC)HCID 24808478—
Reactant(3aR,5R,6S,7R,7aR)-2-(ethylamino)-5-[(4-pyridin-2-yltriazol-1-yl)methyl]-5,6,7,7a-tetrahydro-3aH-pyrano[3,2-d][1,3]thiazole-6,7-diolHCID 178463442—
SolventTetrahydrofuranHCID 8028—
ProductCID 71271091HCID 71271091—

Reaction Conditions

Temperature0 °C

Reaction Steps

The carboxylic acid intermediate of Schemes 1 to 3 was synthesized as follows: To a suspension of (3aR,5R,6S,7R,7aR)-2-(ethylamino)-5-(hydroxymethyl)-5,6,7,7a-tetrahydro-3aH-pyrano[3,2-d]thiazole-6,7-diol (23 g, 93 mmol) in 1:1 THF/aqueous NaHCO3 (1200 mL) was added TEMPO (3.2 g, 20 mmol) and potassium bromide (3.5 g, 30 mmol). The mixture was then cooled to 0° C. and a solution of sodium hypochlorite (190 mL, 9% active chlorine basis) was added, dropwise. After 1 h, additional amounts of sodium hypochlorite solution (95 mL) and TEMPO (1.6 g, 10 mmol) were added. After TLC analysis indicated the reaction was complete, the reaction solution was extracted with diethyl ether (2×250 mL). The aqueous layer was acidified with 5N HCl to pH 5-6, and then concentrated under reduced pressure. The residue was purified by flash chromatography on silica gel using a gradient of methanol/dichloromethane (1% to 50%) to afford the title compound (23 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08884023B2
Source datasetuspto-grants-2014_11
ORD IDord-6e20622b4a4e4d16abdaafa7ac6de133
Source noteuspto-grants-2014_11