Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Aminopropanol | HCID 5126 | — |
| Reactant | HCID 178460299 | HCID 178460299 | — |
| Reactant | HCID 178510530 | HCID 178510530 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178460296 | HCID 178460296 | — |
Reaction Steps
5-[3-(3-(1H-indole-1-carbonyl)phenylamino]-3-hydroxy-N-(1-hydroxypropan-2-yl)isothiazole-4-carboximidamide 6: 5-[3-(3-(1H-indole-1-carbonyl)phenylamino]-3-hydroxyisothaizole-4-carbonitrile 5: (0.362 gm, 1 mmol) was taken into anhydrous EtOH (10 ml) and to this 2-amino-propan-1-ol (0.375 gm, 5 mmol) was added. The reaction mixture was stirred at 80° C. for 16 h., then concentrated to dryness and purified by column chromatography to provide 5-[4-(2,3-dihydro-indole-1-carbonyl)-phenylamino]-3-hydroxy-N-(2-hydroxy-1-methyl-ethyl)-isothiazole-4-carboxamidine 6.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07429667B2 |
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| Source dataset | uspto-grants-2008_09 |
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| ORD ID | ord-448d33eadda545649617d500921c9522 |
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| Source note | uspto-grants-2008_09 |
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