Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Aminopyridine | HCID 10439 | — |
| Reactant | Phenyl chloroformate | HCID 15891 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 18793474 | HCID 18793474 | — |
Reaction Steps
The reaction of a haloformate, such as phenyl chloroformate, and a pyridinylamine generally is carried out by combining a slight excess of haloformate with the pyridine in an organic solvent, such as triethylamine or pyridine, and stirring the mixture for about 1 to about 24 hours at a temperature of about 0° to about 30° C. The product of the reaction, a pyridinyl carbamate, is generally isolated by acidifying the reaction mixture, for instance by the addition of a mineral acid, such as hydrochloric acid or sulfuric acid, and collecting by filtration the precipitate which forms. The carbamate normally needs no further purification, but if desired it can be crystallized from common solvents, such as benzene, acetone, ethyl acetate, and the like.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04600430 |
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| Source dataset | uspto-grants-1986_07 |
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| ORD ID | ord-d0148d236dd6450187585fca893e2f62 |
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| Source note | uspto-grants-1986_07 |
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