HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 728717Generated: October 31, 2026
Isobutylamine → 10-[(2RS)-1-diethylamino-2-propyl]-N-(2-methylpropyl)-2-phenothiazinecarbothioamide
https://huagongshe.com/reaction/728717
Participants
| Role | Name | HCID | Charge |
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| Reactant | Isobutylamine | HCID 6558 | — |
| Reactant | 10-(1-Diethylamino-2-propyl)-2-phenothiazinecarbothioamide | HCID 14536511 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 10-[(2RS)-1-diethylamino-2-propyl]-N-(2-methylpropyl)-2-phenothiazinecarbothioamide | HCID 14536567 | — |
Reaction Steps
Isobutylamine (2.50 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 50° C. The residue obtained is purified by chromatography on a column (height: 16.5 cm; diameter: 2.8 cm) silica gel (0.04-0.06 mm) with a slight excess presof sure of nitrogen (40 kPa), eluting with mixtures of cyclohexane and ethyl acetate in proportions (by volume) of 80:20 (1.5 liters) and 50:50 (1 liter), collecting 50-cc fractions. Fractions 4 to 15 are combined and concentrated to dryness under reduced pressure (30 mm Hg; 4 kPa) at 40° C. to give 10-[(2RS)-1-diethylamino-2-propyl]-N-(2-methylpropyl)-2-phenothiazinecarbothioamide (1.3 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-7b6b84990ceb45cdbcfeb59f1d89c308 |
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| Source note | uspto-grants-1991_09 |
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