HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 979607Generated: October 29, 2026
Dichloromethane → HCID 135626398, compound
https://huagongshe.com/reaction/979607
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | 2-Amino-5-chlorobenzophenone | HCID 12870 | — |
| Reactant | 2-Chloro-3-pyridylamine | HCID 80528 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 135626398 | HCID 135626398 | 15.2% |
Reaction Steps
A mixture of 15.0 g (0.0647 mole) of 2-amino-5-chlorobenzophenone and 9.1 g (0.068 mole) of 3-amino-2-chloropyridine was heated at 200° C. (in an oil bath) for 0.75 hr under nitrogen atmosphere. The mixture was cooled and methylene chloride added. The mixture was stirred for 1 hr then allowed to stand overnight. Brown solid precipitate weighing 8.7 g was separated by filtration. The filtrate was evaporated under reduced pressure. The residue was combined with the brown solid and partitioned with aqueous sodium hydroxide and methylene chloride and crude product isolated as in Example 1, except the crystallizing solvent was ethanol. Recrystallization from ethanol and drying over night at 82° C./0.1 mm Hg gave 3.0 g product; m.p. 156.5°-158.5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04668675 |
|---|
| Source dataset | uspto-grants-1987_05 |
|---|
| ORD ID | ord-518da2e05fae4afebd8a75deba8a8132 |
|---|
| Source note | uspto-grants-1987_05 |
|---|