HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 704192Generated: October 29, 2026
Hydrogen Sulfide → N-Butyl-10-[(2RS)-1-(N-ethyl-N-methylamino)-2-propyl]-2-phenothiazinecarbothioamide
https://huagongshe.com/reaction/704192
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrogen Sulfide | HCID 402 | — |
| Reactant | Butylamine | HCID 8007 | — |
| Reactant | 10-[(2RS)-1-(N-ethyl-N-methylamino)-2-propyl]-2-phenothiazinecarbothioamide | HCID 14536554 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | N-Butyl-10-[(2RS)-1-(N-ethyl-N-methylamino)-2-propyl]-2-phenothiazinecarbothioamide | HCID 14536555 | — |
Reaction Steps
A mixture of 10-[(2RS)-1-(N-ethyl-N-methylamino)-2-propyl]-2-phenothiazinecarbothioamide (2.1 g) and butylamine (8.5 cc) in absolute ethanol (30 cc) is saturated with hydrogen sulphide and heated for 16 hours to a temperature in the region of 100° C. After cooling, the orange solution obtained is concentrated to dryness under reduced pressure (30 mm Hg; 4 kPa) at 40° C. The residual brown oil is purified by chromatography on a column (height: 4 cm; diameter: 3 cm) of silica gel (0.2-0.063 mm), eluting successively with methylene chloride (2 liters) and with a mixture (90:10 by volume) (1 liter) of methylene chloride and methanol and collecting 60-cc fractions. Fractions 36 to 39 are combined and concentrated to dryness under reduced pressure (30 mm Hg; 4 kPa) at 40° C. The residual orange oil (1.8 g) is again purified by chromatography on a column (height: 25 cm; diameter: 4 cm) of silica gel (0.04-0.063 mm) under a slight excess pressure of nitrogen (40 kPa), eluting with mixture (75:25 by volume) (1 liter) of ethyl acetate and cyclohexane and collecting 60-cc fractions. Fractions 5 to 12 are combined and concentrated to dryness under reduced pressure (30 mm Hg; 4 kPa) at 40° C. N-Butyl-10-[(2RS)-1-(N-ethyl-N-methylamino)-2-propyl]-2-phenothiazinecarbothioamide (1.25 g) is thereby obtained in the form of a yellow oil. This product is dissolved in isopropyl ether (100 cc) and treated, dropwise and with stirring, with a 0.28N solution (10.9 cc) of hydrochloric acid in isopropyl ether. After 1 hour's stirring at a temperature in the region of 5° C, the precipitate formed is drained, washed with isopropyl ether (3×10 cc) and dried under reduced pressure (5 mm Hg; 0.68 kPa) at 40° C. N-Butyl-10-[(2RS)-1-(N-methyl-N-ethylamino)-2-propyl]-2-phenothiazinecarbothioamide hydrochloride (1.1 g) is thereby obtained in the form of a yellow solid, m.p. 102° C. (melts forming a paste).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04985419 |
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| Source dataset | uspto-grants-1991_01 |
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| ORD ID | ord-e866030f658c49d8b513656d8693beeb |
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| Source note | uspto-grants-1991_01 |
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