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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Butylamine | HCID 8007 | — |
| Reactant | 10-(1-Diethylamino-2-propyl)-2-phenothiazinecarbothioamide | HCID 14536511 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | N-butyl-10-[(2RS)-1-diethylamino-2-propyl]-2-phenothiazinecarbothioamide | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05049669 |
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| Source dataset | uspto-grants-1991_09 |
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| ORD ID | ord-a868b86390c142639c131d0a28f56794 |
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| Source note | uspto-grants-1991_09 |
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