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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 728714Generated: October 31, 2026

Hydrogen Sulfide → HCID 14536559, compound

https://huagongshe.com/reaction/728714

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen SulfideHCID 402—
ReactantButylamineHCID 8007—
Reactant10-[1-(1-Pyrrolidinyl)-2-propyl]-2-phenothiazinecarbothioamideHCID 14536528—
SolventEthanolHCID 702—
ProductHCID 14536559HCID 14536559—

Reaction Conditions

Temperature120 °C

Reaction Steps

A mixture of 10-[(2RS)-1-(1-pyrrolidinyl)-2-propyl]-2-phenothiazinecarbothioamide (1 g) and butylamine (1.5 cc) in absolute ethanol (20 cc) is saturated with hydrogen sulphide and then heated for 24 hours to a temperature in the region of 120° C. After being cooled, the reaction mixture is concentrated to dryness under reduced pressure (30 mm Hg; 4 kPa) at 40° C. The residue is taken up with distilled water (10 cc) and ethyl acetate (25 cc). After extraction, the organic phase is separated, washed with distilled water (10 cc) and then with saturated aqueous sodium chloride solution (20 cc), dried over potassium carbonate, filtered and concentrated to dryness under reduced pressure (30 mm Hg; 4 kPa) at 40° C. N-Butyl-10-[(2RS)-1-(1-pyrrolidinyl)-2-propyl]-2-phenothiazinecarbothioamide (1.15 g) is thereby obtained in the form of a viscous yellow oil which is subsequently used as it is.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05049669
Source datasetuspto-grants-1991_09
ORD IDord-2dd0a0b811b54968a78b52f9f75a72f9
Source noteuspto-grants-1991_09