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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2423668Generated: October 26, 2026

Ammonia → 5-Methoxy-2-(6-methoxybenzothiazol-2-yl)phenylamine

https://huagongshe.com/reaction/2423668

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantStannous chloride dihydrateHCID 61436—
Reactant2-Chloro-6-methoxybenzothiazoleHCID 273132—
Reactant6-Methoxy-2-(4-methoxy-2-nitrophenyl)benzothiazoleHCID 23087377—
ReactantTributyl(4-methoxy-2-nitrophenyl)tinHCID 23087474—
SolventHydrochloric AcidHCID 313—
SolventEthanolHCID 702—
Product5-Methoxy-2-(6-methoxybenzothiazol-2-yl)phenylamineHCID 2308752275.5%

Reaction Steps

Synthesized from 2-chloro-6-methoxybenzothiazole and tributyl(4-methoxy-2-nitrophenyl)tin according to an analogous synthetic method to Preparation Example 77, to a suspension of the resulting 6-methoxy-2-(4-methoxy-2-nitrophenyl)benzothiazole (695 mg) in ethanol (10 ml) and concentrated hydrochloric acid (2 ml) was added tin(II) chloride dihydrate (1.3 g), and the solution was stirred for 7 hours at room temperature. The solution was neutralized with ammonia solution on an ice bath, then filtered through celite pad, extracted with ethyl acetate, then sequentially washed with water and brine, the solvent was evaporated in vacuo, the resulting solid was washed with a hexane-diethyl ether system to provide the title compound (475 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07960412B2
Source datasetuspto-grants-2011_06
ORD IDord-7268b29f15004a4498089d095450e513
Source noteuspto-grants-2011_06