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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 443834Generated: October 26, 2026

Isopropanol → HCID 12939920, compound

https://huagongshe.com/reaction/443834

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsopropanolHCID 3776—
ReactantDiisopropyl EtherHCID 7914—
Reactant3-Pyridyl isothiocyanateHCID 2737242—
ReactantHCID 12939919HCID 12939919—
SolventEthanolHCID 702—
ProductHCID 12939920HCID 1293992075.4%

Reaction Conditions

Temperature20 °C

Reaction Steps

A solution of 3-isothiocyanatopyridine (1.36 g) in absolute ethanol (40 cc) is added dropwise, at a temperature of about 0° C., to a solution of (RS)-6-hydroxymethyl-4,5,6,7-tetrahydrothieno[3,2-c]pyridine (1.69 g) in absolute ethanol (60 cc). The resulting solution is stirred for 20 hours at a temperature of about 20° C. and the solid formed is then filtered off. The filtrate is evaporated to dryness under reduced pressure (25 mm Hg; 3.3 kPa) at 40° C. and a white solid is obtained which is combined with the solid isolated by filtration. These solids are dissolved in a mixture, heated under reflux, of isopropanol and diisopropyl ether (1:2 by volume; 130 cc) and the solution, after cooling, is kept at +5° C. for 20 hours. The resulting crystals are filtered off, washed with diisopropyl ether (50 cc) and dried at 20° C. under reduced pressure (0.1 mm Hg; 0.013 kPa). (RS)- 6-Hydroxymethyl-5-[(pyrid-3-yl)thiocarbamoyl]-4,5,6,7-tetrahydrothieno[3,2-c]pyridine (2.3 g) is thus obtained in the form of white crystals melting at 186° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04261999
Source datasetuspto-grants-1981_04
ORD IDord-9e6a3750a6cd46748b9b9fe248579ceb
Source noteuspto-grants-1981_04