HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1664220Generated: October 31, 2026
Allylamine → 2-Allylamino-6-methoxy-isonicotinic acid
https://huagongshe.com/reaction/1664220
Participants
| Role | Name | HCID | Charge |
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| Reactant | Allylamine | HCID 7853 | — |
| Reactant | 3-(Allyl-benzyloxycarbonyl-amino)-5-oxazol-2-yl-benzoic acid | HCID 67439318 | — |
| Catalyst | Copper sulfate pentahydrate | HCID 24463 | — |
| Solvent | Citric Acid | HCID 311 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-Allylamino-6-methoxy-isonicotinic acid | HCID 67439626 | — |
Reaction Steps
A mixture of 3.97 ml (52 mmol, 10 eq) allylamine, 0.97 g (5.2 mmol, 1 eq) 2-chloro-6-methoxy-isonicotinic acid (see building block A3) and 1.29 g (5.2 mmol, 1 eq)-copper(II) sulfate pentahydrate in 10 ml water is heated in a closed vessel during 2.5 h at a bath temperature of 160° C. After cooling to rt the mixture is diluted with 400 ml aq 10% citric acid and extracted with EtOAc. The extracts are washed with water and brine, dried over sodium sulfate and the solvents are evaporated at reduced pressure. The residue is dissolved in about 20 ml hot DCM/MeOH (2/1). On addition of about 25 ml of hexane, partial evaporation of the solvents to a volume of about 20 ml and keeping at 4° C. for 4 h the product precipitates and is filtered off and dried in vacuum.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08039455B2 |
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| Source dataset | uspto-grants-2011_10 |
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| ORD ID | ord-0971f7496c86489d975fba27dff40d08 |
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| Source note | uspto-grants-2011_10 |
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