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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1072328Generated: November 2, 2026

Tributyltin Chloride → 7-(Pyrimidin-5-yl)carbonyl-2-(tri-n-butylstannyl)-imidazo[5,1-b]thiazole

https://huagongshe.com/reaction/1072328

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTributyltin ChlorideHCID 15096—
Reactant7-[(Pyrimidin-5-yl)hydroxymethyl]imidazo[5,1-b]thiazoleHCID 22390238—
ReactantLiHMDS tetrahydrofuranHCID 23714775—
CatalystHCID 178418406HCID 178418406—
Product7-(Pyrimidin-5-yl)carbonyl-2-(tri-n-butylstannyl)-imidazo[5,1-b]thiazoleHCID 22390306—

Reaction Steps

A ketone compound (217 mg) was prepared in substantially the same manner as in step b) of Synthesis Example 1, except that 398 mg of 7-[(pyrimidin-5-yl)hydroxymethyl]imidazo[5,1-b]thiazole and 400 mg of manganese dioxide were used as the starting compounds. 7-(Pyrimidin-5-yl)carbonyl-2-(tri-n-butylstannyl)-imidazo[5,1-b]thiazole (68 mg) was prepared in substantially the same manner as in step c) of Synthesis Example 1, except that 46 mg of the ketone compound, 0.124 ml of tri-n-butylstannyl chloride, and 0.900 ml of a 1.0 N lithium bis(trimethylsilyl)amide/THF solution were used as the starting materials.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06908913B2
Source datasetuspto-grants-2005_06
ORD IDord-b6eb9f83521b4fd2963dbc1fa0463c92
Source noteuspto-grants-2005_06