HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1830757Generated: October 26, 2026
2-Isocyanato-1-methoxy-4-methylbenzene → 3-(2-Methoxy-5-methyl-phenyl)-1-methyl-1-pyrazin-2-yl-urea
https://huagongshe.com/reaction/1830757
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Isocyanato-1-methoxy-4-methylbenzene | HCID 4141520 | — |
| Reactant | N-Methylpyrazin-2-amine | HCID 16767478 | — |
| Reactant | Dichloromethane methanol | HCID 21226129 | — |
| Reactant | Ethyl acetate hexane | HCID 21226206 | — |
| Solvent | 1,1-Dichloroethane | HCID 6365 | — |
| Product | 3-(2-Methoxy-5-methyl-phenyl)-1-methyl-1-pyrazin-2-yl-urea | HCID 22046431 | — |
Reaction Steps
To a 0.3 M stirred solution of 2-methylaminopyrazine (1 equiv.) in dichloroethane at room temperature under nitrogen was added 2-methoxy-5-methylphenylisocyanate (1 equiv.). The reaction was warmed to 80° C. overnight and then cooled to room temperature. In most cases, the product precipitated and was isolated by filtration. Alternatively the product could be isolated by silica gel chromatography using EtOAc/hexane or CH2Cl2/MeOH as eluant. 1H-NMR (400 MHz, CDCl3) δ8.57 (s, 1H), 8.32 (s, 1H), 8.31 (s, 1H), 8.17 (s, 1H), 6.80 (i, 2H), 3.90 (s, 3H), 3.56 (s, 3H), 2.32 (s, 3H). LRMS (ESI, Positive) m/e 273.2 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07067506B2 |
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| Source dataset | uspto-grants-2006_06 |
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| ORD ID | ord-7757c99411094b4eafe7b8902b065176 |
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| Source note | uspto-grants-2006_06 |
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