Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 2-Chloroaniline | HCID 7240 | — |
| Reactant | Boric Acid | HCID 7628 | — |
| Reactant | HCID 12401526 | HCID 12401526 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Product | HCID 12401527 | HCID 12401527 | — |
Reaction Steps
22.32 g of 2-(p-formylphenyl)-s-triazolo[1,5-a]pyridine (II), 14.03 g of o-chloroaniline and 1 g of boric acid in 350 ml of xylene are refluxed for 2 hours, the water formed being distilled off. The mixture is cooled to 60° C., 450 ml of methanol are added and the resulting mixture is further cooled to -10° C. The product which has precipitated is filtered off with suction, washed with 100 ml of cold methanol and dried. This gives 26.3 g (79.1% of theory) of compound (101) in the form of a pale beige powder with a melting point of 135° to 136° C. After recrystallising twice from methanol, 22.2 g (66.7% of theory) of small, pale yellow, glossy needles with a melting point of 135° to 136° C. are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04113937 |
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| Source dataset | uspto-grants-1978_09 |
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| ORD ID | ord-6e7b2c53d8cb4118b7be9be3cee4664a |
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| Source note | uspto-grants-1978_09 |
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