HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1684936Generated: October 25, 2026
N,N-Dimethylglycine → Methyl 3-(6-aminopyridin-3-yloxy)benzoate
https://huagongshe.com/reaction/1684936
Participants
| Role | Name | HCID | Charge |
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| Reactant | N,N-Dimethylglycine | HCID 673 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | 2-Amino-5-bromopyridine | HCID 70622 | — |
| Reactant | Methyl 3-Hydroxybenzoate | HCID 88068 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | Methyl 3-(6-aminopyridin-3-yloxy)benzoate | HCID 67263263 | 51.2% |
Reaction Steps
A procedure described by D. Ma and Q. Cai (Org. Lett. 3799, 2003) was followed. To a solution of 5-bromopyridin-2-amine (346 mg, 2 mmol) in dioxane (10 mL) were added methyl 3-hydroxybenzoate (400 mg, 2.6 mmol), CuI (50 mg), N,N-dimethylglycine (60 mg) and Cs2CO3 (1.0 g). The resulting mixture was heated to 120° C. for 5 h, then cooled and partitioned between water and dichloromethane. The organic layer was separated, dried, and concentrated. The residue was purified by silica gel column eluting with ethyl acetate in dichloromethane (1:1) to obtain methyl 3-(6-aminopyridin-3-yloxy)benzoate (250 mg, 50%) as an oil. LC/MS; (M+H)+=245.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08148361B2 |
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| Source dataset | uspto-grants-2012_04 |
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| ORD ID | ord-1a2cae8af1bd4feda962544efec2b2ed |
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| Source note | uspto-grants-2012_04 |
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