HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 26193Generated: October 26, 2026
4-Chlorophenyl Isocyanate → 3,5-dichloro-N-[(4-chlorophenylamino)carbonyl]-4-pyridinecarboxamide
https://huagongshe.com/reaction/26193
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Chlorophenyl Isocyanate | HCID 7693 | — |
| Reactant | 3,5-Dichloroisonicotinamide | HCID 2802911 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Product | 3,5-dichloro-N-[(4-chlorophenylamino)carbonyl]-4-pyridinecarboxamide | HCID 21325114 | — |
Reaction Steps
A reaction vessel was charged with sixty-eight grams (0.36 mole) of 3,5-dichloro-4-pyridinecarboxamide, 55.5 grams (0.36 mole) of p-chlorophenyl isocyanate, and 1200 milliliters of xylene. The solution was heated under reflux with stirring for three hours. A small amount of impurity was removed by filtering the hot reaction mixture. On cooling in an ice water bath, a solid precipitated. The precipitated product was collected by suction filtration, washed with cold xylene and dried in a vacuum oven at about 70° C. The dried crude product was purified by recrystallization from 90 percent aqueous acetic acid. The yield was 81 grams (66 percent of theoretical) of white needles melting at 225°-227° C. Nuclear magnetic resonance spectral data confirmed the structure as being ##STR12##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04148902 |
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| Source dataset | uspto-grants-1979_04 |
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| ORD ID | ord-2f12c5c348974c2395d0688146a80d43 |
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| Source note | uspto-grants-1979_04 |
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