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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 728708Generated: October 28, 2026

Butylamine → N-butyl-10-[(2RS)-1-diethylamino-2-propyl]-2-phenothiazinecarbothioamide

https://huagongshe.com/reaction/728708

Reaction equation

Participants

RoleNameHCIDCharge
ReactantButylamineHCID 8007—
Reactant10-(1-Diethylamino-2-propyl)-2-phenothiazinecarbothioamideHCID 14536511—
SolventEthanolHCID 702—
ProductN-butyl-10-[(2RS)-1-diethylamino-2-propyl]-2-phenothiazinecarbothioamideHCID 14536544—

Reaction Steps

n-Butylamine (2.4 cc) is added to a solution of 10-[(2RS)-1-diethylamino-2-propyl]-2-phenothiazinecarbothioamide (1.86 g) in absolute ethanol (25 cc). The mixture is brought to 150° C. for 16 hours and then concentrated to dryness under reduced pressure (30 mm Hg; 4 kPa) at 40° C. The residue obtained is purified by chromatography on a column (height: 17 cm; diameter: 2.6 cm) of silica gel (0.04-0.06 mm) with a slight excess pressure of nitrogen (40 kPa), eluting with mixtures of cyclohexane and ethyl acetate in proportions (by volume) of 90:10 (250 cc), 80:20 (500 cc) and 50:50 (750 cc) and then with pure ethyl acetate (750 cc), collecting 50-cc fractions. Fractions 10 to 18 are combined and concentrated to dryness under reduced pressure (30 mm Hg; 4 kPa) at 40° C. to give N-butyl-10-[(2RS)-1-diethylamino-2-propyl]-2-phenothiazinecarbothioamide (0.96 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05049669
Source datasetuspto-grants-1991_09
ORD IDord-a868b86390c142639c131d0a28f56794
Source noteuspto-grants-1991_09