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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1701891Generated: November 2, 2026

Methane → N-methyl-2-(pyrid-2-yl)-tetrahydrothiopyran-2-carbothioamide

https://huagongshe.com/reaction/1701891

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethaneHCID 297—
ReactantMethylamineHCID 6329—
ReactantMethyl 2-(pyrid-2-yl)-tetrahydrothiopyran-2-carbodithioateHCID 13043960—
SolventEthanolHCID 702—
ProductN-methyl-2-(pyrid-2-yl)-tetrahydrothiopyran-2-carbothioamideHCID 13139530—

Reaction Conditions

Temperature20 °C

Reaction Steps

A 33% (weight/volume) solution of methylamine in ethanol (7.5 cc) is added dropwise and in the course of 15 minutes to a solution of methyl 2-(pyrid-2-yl)-tetrahydrothiopyran-2-carbodithioate (9 g) in ethanol (60 cc), kept at a temperature of about 20° C. The solution is then stirred for 16 hours at a temperature of about 20° C. The resulting crystals are filtered off, washed twice with ethanol (20 cc in total) and dried under reduced pressure (20 mm Hg; 2.7 kPa) at a temperature of about 20° C. A crystalline crude product (7.8 g) is thus obtained, which is redissolved in boiling ethanol (96 cc); decolourising charcoal (0.4 g) is added to the solution thus obtained, which is filtered hot, and the filtrate is then cooled for 30 minutes at 0° C. The resulting crystals are filtered off, washed twice with ethanol (20 cc in total) and dried under reduced pressure (1 mm Hg; 0.13 kPa) at 45° C. N-Methyl-2-(pyrid-2-yl)-tetrahydrothiopyran-2-carbothioamide (6.3 g), melting at 153° C., is thus obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04379154
Source datasetuspto-grants-1983_04
ORD IDord-0a8c3f18938e4f8db86b25368e529eef
Source noteuspto-grants-1983_04