Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | 2-Iodobenzohydrazide | HCID 615675 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 19170012 | HCID 19170012 | 77% |
Reaction Steps
2-Iodobenzohydrazide (1.38 g, 5.27 mmol) obtained in Step 1 of Example 114 was dissolved in dichloromethane (50 mL), and the mixture was stirred at 0° C. for 1.5 hours after adding pyridine (0.639 mL, 7.90 mmol) and acetyl chloride (0.412 mL, 5.79 mmol). The precipitated solid was filtered off, and the resulting solid was dried under reduced pressure to give N′-acetyl-2-iodobenzohydrazide (1.23 g, 77%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07998954B2 |
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| Source dataset | uspto-grants-2011_08 |
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| ORD ID | ord-964784db775d4e29a25e91b4cee09636 |
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| Source note | uspto-grants-2011_08 |
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