HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2274735Generated: November 1, 2026
Hydroxylamine → 2,5-dichloro-N-hydroxy-4,6-dimethylpyridine-3-carboximidamide
https://huagongshe.com/reaction/2274735
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydroxylamine | HCID 787 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | 1,10-Phenanthroline hydrate | HCID 21226 | — |
| Reactant | 2,5-Dichloro-4,6-dimethylpyridine-3-carbonitrile | HCID 334852 | — |
| Solvent | Methanol--water (1/1) | HCID 22242641 | — |
| Product | 2,5-dichloro-N-hydroxy-4,6-dimethylpyridine-3-carboximidamide | HCID 46205171 | — |
Reaction Steps
A suspension of 2,5-Dichloro-4,6-dimethyl-nicotinonitrile (45.0 kg) and 50% hydroxylamine (59.2 kg) in the presence of catalytic amount of 1,10-phenanthroline monohydrate (0.680 kg) in methanol/water (214 kg/362 kg) is heated to 70-80° C. The mixture is agitated at 70-80° C. Water (353 kg) is added slowly into the resulting solution while the temperature is maintained at >79° C. The solution is cooled to 75° C. with stirring resulting in crystallization of (Z)-2,5-dichloro-N′-hydroxy-4,6-dimethylnicotinimidamide. The suspension is further cooled to 20° C., the solid is filtered off and the wet cake is washed with water (160 kg). (Z)-2,5-dichloro-N′-hydroxy-4,6-dimethylnicotinimidamide is dried under vacuum at max. 60° C. until residual water level is max 0.15% (KF).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09126988B2 |
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| Source dataset | uspto-grants-2015_09 |
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| ORD ID | ord-1ed0d7dd83264926b7db9c744945c45b |
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| Source note | uspto-grants-2015_09 |
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