HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2284595Generated: October 29, 2026
Ethoxalyl chloride → HCID 86715507, compound
https://huagongshe.com/reaction/2284595
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethoxalyl chloride | HCID 20884 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 86715505 | HCID 86715505 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 86715507 | HCID 86715507 | — |
Reaction Steps
To a stirring solution of (2′-(4-fluoro-3-methylphenyl)-[3,3′-bipyridin]-6-yl)methanamine (2.0 g) in CH2Cl2 (30 mL) under nitrogen atmosphere, i-Pr2NEt (2.6 mL) was added and stirred for 10 min at room temperature. Ethyl 2-chloro-2-oxoacetate (1.1 mL) as neat was added dropwise for 10 min. After 1 h, the reaction mixture was concentrated, partitioned between CH2Cl2 (75 mL)/aq. NaCl (20 mL) and the organic layer was separated. Usual workup and purification by chromatography (Combiflash® companion System® with RediSep® silica gel column 40 g and 50-100% EtOAc/hexanes as an elutant) provided 1.4 g of ethyl 2-(((2′-(4-fluoro-3-methylphenyl)-[3,3′-bipyridin]-6-yl)methyl)amino)-2-oxoacetate as an off-white solid. 1H NMR (300 MHz, DMSO-d6): δ 9.41 (t, J=6.2 Hz, 1H), 8.67 (dd, J=4.7, 1.7 Hz, 1H), 8.30 (dd, J=2.4, 0.9 Hz, 1H), 7.87 (dd, J=7.8, 1.7 Hz, 1H), 7.56 (dd, J=8.1, 2.3 Hz, 1H), 7.49 (dd, J=7.8, 4.8 Hz, 1H), 7.29-7.22 (m, 2H), 6.98 (dd, J=7.7, 1.1 Hz, 2H), 4.42 (d, J=6.1 Hz, 2H), 4.23 (q, J=7.1 Hz, 2H), 2.21-2.09 (m, 3H), 1.26 (t, J=7.1 Hz, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09145433B2 |
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| Source dataset | uspto-grants-2015_09 |
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| ORD ID | ord-39c376106c9a45b3857134673e08bb64 |
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| Source note | uspto-grants-2015_09 |
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