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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 555891Generated: October 30, 2026

Benzo(d)thiazol-2-amine → HCID 59351145, compound

https://huagongshe.com/reaction/555891

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzo(d)thiazol-2-amineHCID 8706—
ReactantSodium CarbonateHCID 10340—
ReactantDiphenylphosphineHCID 70017—
ReactantHCID 59351380HCID 59351380—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventTolueneHCID 1140—
ProductHCID 59351145HCID 59351145—

Reaction Conditions

Temperature100 °C

Reaction Steps

To a mixture of tris(dibenzylideneacetone)dipalladium(0) (0.021 g, 0.023 mmol), Na2CO3 (0.081 g, 0.76 mmol), 9,9-dimethyl-9H-xanthene-4,5-diyl)bis(diphenylphosphine (0.040 g, 0.069 mmol), benzo[d]thiazol-2-amine (0.110 g, 0.732 mmol), and 1-(4-(3-(6-chloropyridin-3-yloxy)pyrazin-2-yl)piperidin-1-yl)ethanone (0.182 g, 0.547 mmol) was added PhMe (3 mL). The reaction mixture was degassed and heated to 100° C. for 40 h. The reaction mixture was diluted with Teac and the organic phase was washed with water (1×), brine (1×), dried over MgSO4, filtered, and concentrated. Purification by flash column chromatography on silica gel (10% to 80% Teac (10% MeOH) in hexanes) gave 1-(4-(3-(6-(benzo[d]thiazol-2-ylamino)pyridin-3-yloxy)pyrazin-2-yl)piperidin-1-yl)ethanone as a white solid. MS (ESI, pos. ion) m/z: 447.2 (M+1). IC50 (uM) ++.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08053438B2
Source datasetuspto-grants-2011_11
ORD IDord-ed54e3f32ec84b4ca200e2fa70919cd6
Source noteuspto-grants-2011_11