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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 731637Generated: October 31, 2026

Methyl 6-aminonicotinate → HCID 24738996, compound

https://huagongshe.com/reaction/731637

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 6-aminonicotinateHCID 737487—
Reactant4-(Bromoacetyl)-5-methyl-3-phenylisoxazoleHCID 2735531—
ProductHCID 24738996HCID 2473899638%

Reaction Steps

As described for Example 1, 4-(bromoacetyl)-5-methyl-3-phenylisoxazole (commercially available) (140 mg, 0.5 mmol) was converted, using methyl 6-aminonicotinate instead of 2-aminopyridine, to the title compound (64 mg, 38%) which was obtained as a light yellow solid. MS: m/e=334.3 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07585874B2
Source datasetuspto-grants-2009_09
ORD IDord-d499200678a74475ae5ebc8f6b17a497
Source noteuspto-grants-2009_09