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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1744814Generated: November 1, 2026

Pyridine → (1S,4S)-2-Oxa-5-aza-bicyclo[2.2.1]heptane-5-carboxylic Acid (4-methoxy-7-morpholin-4-yl-benzothiazol-2-yl)-amide

https://huagongshe.com/reaction/1744814

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantSodium CarbonateHCID 10340—
ReactantPhenyl chloroformateHCID 15891—
Reactant(1S,4S)-2-oxa-5-azabicyclo[2.2.1]heptane hydrobromideHCID 11159293—
Reactant4-Methoxy-7-morpholinobenzo[d]thiazol-2-amineHCID 11402861—
SolventDichloromethaneHCID 6344—
Product(1S,4S)-2-Oxa-5-aza-bicyclo[2.2.1]heptane-5-carboxylic Acid (4-methoxy-7-morpholin-4-yl-benzothiazol-2-yl)-amideHCID 1118845135%

Reaction Steps

To a solution of 4-methoxy-7-morpholin-4-yl-benzothiazol-2-ylamine (265 mg, 1.0 mmol) in dichloromethane (15 ml) is subsequently added pyridine (0.24 ml, 3.0 mmol) and phenyl chloroformate (0.15 ml, 1.2 mmol) and the resulting solution stirred for 45 min at ambient temperature. Then (1S,4S)-2-oxa-5-aza-bicyclo[2.2.1]heptane (490 mg, 3.6 mmol) is added and the mixture stirred at ambient temperature for 15 min and at 40° C. for 2.5 h. After cooling to ambient temperature, saturated aqueous sodium carbonate (15 ml) is added, the organic phase is separated, dryed and the solvent evaporated in vacuo. Flash chromatography (silica, eluent: dichloromethane containing methanol (gradient from 0 to 5%)) afforded the title compound as white crystals (135 mg, 35% yield). MS: m/e=391(M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07019001B2
Source datasetuspto-grants-2006_03
ORD IDord-ad29433b1f2d4bd8ac4302f564cf4b9b
Source noteuspto-grants-2006_03