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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 585746Generated: October 31, 2026

4-Aminopyridine → HCID 22337417, compound

https://huagongshe.com/reaction/585746

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-AminopyridineHCID 1727—
Reactant2-Chloro-1-methylpyridinium iodideHCID 167069—
ReactantHCID 22337389HCID 22337389—
ProductHCID 22337417HCID 22337417461.4%

Reaction Steps

By a similar reaction operation as in Starting Material Synthetic Example 53 using 4-(tert-butoxycarbonylamino)-8-methylthiochromane-7-carboxylic acid (400 mg), 4-aminopyridine (91.9 mg) and 2-chloro-1-methylpyridinium iodide (474 mg), the objective 4-(tert-butoxycarbonylamino)-8-methyl-N-(4-pyridyl)thiochromane-7-carboxamide (1.80 g) was obtained as colorless crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06933305B2
Source datasetuspto-grants-2005_08
ORD IDord-879f2c0c9e344b129829c9f3388a1675
Source noteuspto-grants-2005_08