HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 70980720, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2,4-Dimethoxybenzylamine | HCID 597250 | — |
| Reactant | Ethyl 2-[(6-chloro-3-nitro-2-pyridinyl)oxy]acetate | HCID 13245756 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 70980720 | HCID 70980720 | 79.1% |
Reaction Steps
To a cooled (˜10° C.) solution of (6-chloro-3-nitro-pyridin-2-yloxy)-acetic acid ethyl ester (8.0 g, 30.8 mmol) in MeCN (80 mL) was added a solution of triethylamine (6.4 mL, 46 mmol) and 2,4-dimethoxybenzylamine (5.5 mL, 37 mmol). The mixture was then stirred for 16 hours at ambient temperature and then concentrated in vacuo. The residue was partitioned between EtOAc and aqueous potassium hydrogenphosphate solution. The EtOAc layer was then washed with brine, dried over MgSO4, filtered and concentrated in vacuo. The residue was purified using SiO2 chromatography (10-50% EtOAc/Petrol) to give [6-(2,4-dimethoxy-benzylamino)-3-nitro-pyridin-2-yloxy]acetic acid ethyl ester (9.53 g) as a yellow solid. MS: [M+H]+ 392
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09155743B2 |
| Source dataset | uspto-grants-2015_10 |
| ORD ID | ord-e92a3be54b6d4d42b4c82659aa8857bc |
| Source note | uspto-grants-2015_10 |