Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Phenyl chloroformate | HCID 15891 | — |
| Reactant | 2-Benzothiazolamine, 6-bromo- | HCID 85149 | — |
| Solvent | Dimethylacetamide | HCID 31374 | — |
| Product | HCID 86688544 | HCID 86688544 | 62% |
Reaction Steps
Phenyl chloroformate (3.49 g, 22.3 mmol) was dissolved in acetonitrile (20 mL), and 2-amino-6-bromobenzothiazole (5.06 g, 22.1 mmol) dissolved in dimethylacetamide (20 mL) was added thereto, followed by stirring at 50° C. for 17 hours. The compound (5.51 g, 22.3 mmol) obtained in Example 1 (2) and triethylamine (hereinafter referred to as Et3N) (12.8 mL, 91.9 mmol) were added to the resulting mixture, followed by stirring at 70° C. for 5 hours. Water (120 mL) was added to the resulting mixture, and the precipitate was collected by filtration and washed with ethanol, thereby giving the title compound (5.84 g, 62%) as a brown solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09181183B2 |
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| Source dataset | uspto-grants-2015_11 |
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| ORD ID | ord-7046813cd971469fbff5cdb9966cb33c |
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| Source note | uspto-grants-2015_11 |
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