HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 453387Generated: October 25, 2026
2,5-Pyridinediamine → Methyl 3-((6-aminopyridin-3-yl)carbamoyl)-4-methylbenzoate
https://huagongshe.com/reaction/453387
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2,5-Pyridinediamine | HCID 20314 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Reactant | 5-(Methoxycarbonyl)-2-methylbenzoic acid | HCID 22999486 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Methyl 3-((6-aminopyridin-3-yl)carbamoyl)-4-methylbenzoate | HCID 68453452 | — |
Reaction Steps
In a round-bottomed flask was charged 5-(methoxycarbonyl)-2-methylbenzoic acid (0.2 g, 1.0 mmol), dicloromethane (3 ml), n,n-diisopropylethylamine (0.7 ml, 4.0 mmol), HOBt (0.16 g, 1.2 mmol), 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (0.24 g, 1.2 mmol), and 2,5-diaminopyridine (0.11 g, 1.0 mmol) in that order. The reaction mixture was stirred at RT under N2 for 18 h. The reaction was partitioned between DCM (30 ml) and brine (20 mL). The aqueous layer was back extracted with DCM (3×15 mL) and the combined DCM layer was dried (Na2SO4) and concentrated. The crude product was dissolved in MeOH and absorbed on silica gel, pyrified by chromatography through a Redi-Sep 40 g column, eluting with a gradient of 0% to 10% MeOH in CH2Cl2, to provide methyl 3-((6-aminopyridin-3-yl)carbamoyl)-4-methylbenzoate as a tan solid. MS (ESI, pos. ion) m/z: 286.2 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08492404B2 |
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| Source dataset | uspto-grants-2013_07 |
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| ORD ID | ord-de5888cc3dfe4f2991bdaf9e33e27356 |
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| Source note | uspto-grants-2013_07 |
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