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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2294602Generated: November 4, 2026

Methyl isothiocyanate → Aprikalim

https://huagongshe.com/reaction/2294602

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl isothiocyanateHCID 11167—
ReactantAmmonium ChlorideHCID 25517—
ReactantSodiumHCID 5360545—
Reactant(1R,2S)-2-(3-pyridyl)tetrahydro-2H-thiopyran 1-oxideHCID 15147288—
CatalystFerric nitrateHCID 25251—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
ProductAprikalimHCID 9571083485.1%

Reaction Conditions

Temperature20 °C

Reaction Steps

Ammonia gas is condensed at -50° C. to obtain 2 ml of liquid ammonia, which is treated with iron (III) nitrate (0.0015 g), followed by sodium metal (0.02 g). The solution turns blue and then dark grey after 20 minutes. It is then treated with a solution of (1R,2S)-2-(3-pyridyl)tetrahydro-2H-thiopyran 1-oxide (0.06 g) in tetrahydrofuran (8 ml) during 2 minutes, at -40° C. The mixture is stirred for 2 minutes and is then treated with a solution of methyl isothiocyanate (0.033 g) in tetrahydrofuran (2 ml), by syringe. The reaction mixture is stirred for 5 minutes at -35° C. and then treated with ammonium chloride (0.05 g) and warmed to 20° C. The mixture is treated with methanol (0.3 ml) and evaporated under reduced pressure. The residue is partitioned between brine (10 ml) and dichloromethane (3×30 ml). The organic phases are combined and dried with magnesium sulphate, filtered and evaporated under reduced pressure, to give (1R,2R)-2-(3-pyridyl)-N-methyltetrahydro-2H-thiopyran-2-carbothioamide 1-oxide (0.4 g; 99% ee) in the form of a white solid, m.p. 215° C. [NMR (CDCl3): 8.7(s,1H); 8.5(s,2H); 8.1(d,1H); 7.3(s,1H); 3.8(s,1H); 3.1(d,3H); 2.8(s,1H); 2.4-1.5(m,6H)].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05688954
Source datasetuspto-grants-1997_11
ORD IDord-289a424130964fda9bad0194e3367749
Source noteuspto-grants-1997_11