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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1693525Generated: November 1, 2026

2-(Tributylstannyl)-1,3-benzothiazole → HCID 11676877, compound

https://huagongshe.com/reaction/1693525

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(Tributylstannyl)-1,3-benzothiazoleHCID 3762392—
ReactantHCID 57898160HCID 57898160—
CatalystHCID 178418397HCID 178418397—
SolventTolueneHCID 1140—
ProductHCID 11676877HCID 11676877—

Reaction Conditions

Temperature100 °C

Reaction Steps

A reaction tube charged with 6-chloro-5-(4-chloro-phenyl)-1-phenyl-1,5-dihydro-pyrazolo[3,4-d]pyrimidin-4-one (20.0 mg, 0.056 mmol) and Pd(PPh3)4 (6.5 mg, 0.0056 mmol) is purged with nitrogen. A solution of 2-tributylstannanyl-benzothiazole (47.6 mg, 0.112 mmol) in anhydrous toluene (1.0 mL) is added via syringe. The reaction mixture is heated at 100° C. for 2 days. After removal of the solvent, the residue is purified by preparative LCMS to provide the title compound; 1H NMR (CDCl3, 400 MHz) δ 8.36 (s, 1H), 8.21 (d, 2H), 7.90 (t, 1H), 7.69 (t, 1H), 7.59 (t, 2H), 7.46-7.40 (m, 5H), 7.24 (d, 2H); HPLC-MS calculated for C24H14ClN5OS (M+H+) 456.1. Found 456.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08158634B2
Source datasetuspto-grants-2012_04
ORD IDord-5e0c7bbcff5147e3b6f35f5cefcb68d0
Source noteuspto-grants-2012_04