HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 979595Generated: October 25, 2026
Dichloromethane → [2-[(3-Amino-2-pyridinyl)amino]-4-chlorophenyl]phenylmethanone
https://huagongshe.com/reaction/979595
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | 2-Amino-4'-chlorobenzophenone | HCID 76166 | — |
| Reactant | 2-Chloro-3-pyridylamine | HCID 80528 | — |
| Product | [2-[(3-Amino-2-pyridinyl)amino]-4-chlorophenyl]phenylmethanone | HCID 15586654 | — |
Reaction Steps
A stirred mixture of 23.2 g (0.1 mole) of 2-amino-4'-chlorobenzophenone and 14.2 g (0.11 mole) of 3-amino-2-chloropyridine was heated at 180° C. under nitrogen atmosphere for 2.5 hr. The mixture solidified upon cooling to room temperature and was broken up with a spatula. The solid was suspended in 100 ml of methylene chloride and collected by filtration. The filter cake was dissolved in a mixture of water-methanol, basified with 3N sodium hydroxide and extracted twice with methylene chloride. The combined methylene chloride extracts were dried over magnesium sulfate and evaporated under reduced pressure. The residue which had crystallized was triturated in isopropyl ether and the solid (16.7 g) collected by filtration. A 3 g sample was recrystallized from isopropyl ether to give 1.6 g product; m.p. 153°-155° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04668675 |
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| Source dataset | uspto-grants-1987_05 |
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| ORD ID | ord-0ae655d2656c470ca43a089a7d82712c |
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| Source note | uspto-grants-1987_05 |
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