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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 628313Generated: October 29, 2026

2-(Tributylstannyl)-1,3-thiazole → 1-benzyl-5-chloro-2-(1,3-thiazol-2-yl)-1H-pyrrolo[3,2-b]pyridine

https://huagongshe.com/reaction/628313

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(Tributylstannyl)-1,3-thiazoleHCID 2763259—
Reactant1-benzyl-2-bromo-5-chloro-1H-pyrrolo[3,2-b]pyridineHCID 118159511—
CatalystHCID 178418397HCID 178418397—
SolventTolueneHCID 1140—
Product1-benzyl-5-chloro-2-(1,3-thiazol-2-yl)-1H-pyrrolo[3,2-b]pyridineHCID 118159544—

Reaction Conditions

Temperature110 °C

Reaction Steps

A mixture of 1-benzyl-2-bromo-5-chloro-1H-pyrrolo[3,2-b]pyridine (0.10 g, 0.31 mmol, from Example 62, Step 2) and 2-(tributylstannyl)-1,3-thiazole (0.12 g, 0.31 mmol, Aldrich) in toluene (6.0 mL) was degassed by a stream of nitrogen through the solution. Tetrakis(triphenylphosphine)palladium(0) (36 mg, 0.031 mmol) was added and the mixture was heated to 110° C. for 4 hours. Toluene was removed in vacuo and the residue was dissolved in MeCN, filtered, and purified via preparative HPLC-MS (C18 eluting with a gradient of MeCN and H2O containing 0.15% NH4OH). Yield: (33 mg, 32%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09309246B2
Source datasetuspto-grants-2016_04
ORD IDord-0d10864239d9469d91cfbdb33ba616d8
Source noteuspto-grants-2016_04