Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | 2-Aminothiophenol | HCID 8713 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Benzothiazoline | HCID 96588 | — |
| Reactant | HCID 86668184 | HCID 86668184 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 68108693 | HCID 68108693 | — |
Reaction Steps
2,3-dihydro-1,3-benzothiazole synthesized from 2-aminobenzenethiol (278 mg) and 37% formalin (0.18 mL) in the same manner as in Example 1 was dissolved in dichloromethane (6.5 mL), and diisopropylethylamine (0.50 mL) and 3-chloro-4-methoxy-5-trifluoromethoxybenzoyl chloride (436 mg) were added to the solution, and then the mixture was stirred at room temperature for 1 hour. The solvent was distilled off under reduced pressure and water was added, and then the mixture was extracted with ethyl acetate. The organic layer was washed with 1N hydrochloric acid, 1N sodium hydroxide and saturated brine, and then dried over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure and the obtained residue was used for the synthesis of (k).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08367843B2 |
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| Source dataset | uspto-grants-2013_02 |
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| ORD ID | ord-93f3557f041a47548bc951987cab0c63 |
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| Source note | uspto-grants-2013_02 |
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