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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1003146Generated: October 31, 2026

Pyridine → HCID 15869092, compound

https://huagongshe.com/reaction/1003146

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantPivaloyl chlorideHCID 62493—
Reactant2-Cyano-6-hydroxybenzothiazoleHCID 9881912—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 15869092HCID 1586909292.2%

Reaction Steps

A solution of 2-cyano-6-hydroxybenzothiazole (2.1 g, 12.5 mmol) in 30 mL of dry THF under inert atmosphere was treated with pyridine (2.0 g, 25 mmol) followed by pivaloyl chloride (1.95 g, 16.2 mmol). This reaction was stirred 15 h at room temperature. The reaction mixture was then diluted with 100 mL of distilled water, and this solution was extracted with ethyl acetate (4×50 mL). The combined organics were washed with aqueous sodium bicarbonate (2×100 mL) and distilled water (1×100 mL), then dried over Na2SO4 and concentrated under reduced pressure to afford 3.0 g of a thick oil. This material was chromatographed on silica gel and 1.8 g of the product was eluted with 10% ethyl acetate/hexanes. 1H NMR (CDCl3): δ 1.39 (s, 9H); 7.34-7.38 (m, 1H); 7.74-7.75 (d, 1H) ; 8.20-8.23 (d, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06045991
Source datasetuspto-grants-2000_04
ORD IDord-924151fd63164ed0aea41915ab73ed2b
Source noteuspto-grants-2000_04