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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1698073Generated: October 30, 2026

Sodium Carbonate → 2-(6-Methoxypyridin-3-yl)-1,3-benzothiazol-6-amine

https://huagongshe.com/reaction/1698073

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant(6-Methoxypyridin-3-yl)boronic acidHCID 2734368—
Reactant2-Bromobenzo[d]thiazol-6-amineHCID 52987807—
CatalystBis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
SolventOxolane--water (1/1)HCID 21881883—
Product2-(6-Methoxypyridin-3-yl)-1,3-benzothiazol-6-amineHCID 2480356596.3%

Reaction Conditions

Temperature140 °C

Reaction Steps

A mixture of 2-bromo-1,3-benzothiazol-6-amine (53 mg, 0.23 mmol), 2-methoxy-5-pyridineboronic acid (50 mg, 0.327 mmol), Pd(dppf)Cl2*DCM (8 mg, 0.01 mmol) and sodium carbonate (0.1 g, 1 mmol) in THF/water (9:1, 3 mL) was heated at 140° C. for 10 minutes in a microwave reactor under argon atmosphere. The mixture was filtered and washed with THF/water (9:1). After having added DCM to the filtrate, the organic layer was washed with brine, dried (Na2SO4), filtered and concentrated. The crude product was purified by flash column chromatography (20 to 70% ethyl acetate in heptane), to yield the title compound (57 mg) as an off-white solid. 1H NMR (CHLOROFORM-d) δ 8.68 (d, 1H) 8.16 (dd, 1H) 7.74 (d, 1H) 7.06 (d, 1H) 6.70-6.81 (m, 2H) 3.94 (s, 3H) 3.77 (s, 2H); MS m/z (M+H) 258.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08163928B2
Source datasetuspto-grants-2012_04
ORD IDord-659e8d2bd817477f9fb1ccc4913eba1b
Source noteuspto-grants-2012_04