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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1809563Generated: October 30, 2026

Ammonium Chloride → HCID 57742595, compound

https://huagongshe.com/reaction/1809563

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
Reactant7-Chlorothieno[3,2-b]pyridineHCID 11275251—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantHCID 66995289HCID 66995289—
SolventDimethyl SulfoxideHCID 679—
ProductHCID 57742595HCID 5774259595.1%

Reaction Steps

A 250 mL flask was charged with tert-butyl 4-(5-(5-(3-methoxy-3-oxopropylthio)-3-phenoxypyridin-2-ylamino)-1,2,4-thiadiazol-3-yl)piperidine-1-carboxylate (10 g, 17 mmol), 7-chlorothieno[3,2-b]pyridine (3.6 g, 21 mmol), and DMSO (125 mL). Nitrogen was bubbled vigorously through the solution for 10 minutes. Potassium 2-methylpropan-2-olate (5.9 g, 52 mmol) was added and the reaction was stirred at ambient temperature under nitrogen for 5 hours. The reaction was poured into saturated aqueous NH4Cl and extracted with EtOAc (1×500 mL). The organic layer was washed with water and brine, dried with sodium sulfate, filtered and concentrated in vacuo. The residue was purified on silica (50 to 75% EtOAc in hexanes) to afford tert-butyl 4-(5-(3-phenoxy-5-(thieno[3,2-b]pyridin-7-ylthio)pyridin-2-ylamino)-1,2,4-thiadiazol-3-yl)piperidine-1-carboxylate (10 g, 92% yield) as a white foam.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08362037B2
Source datasetuspto-grants-2013_01
ORD IDord-219e5191ba654aa7a786cae6828eaf51
Source noteuspto-grants-2013_01