HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2401709Generated: October 30, 2026
2,4-Dimethoxybenzylamine → Ethyl 4-cyano-5-[(2,4-dimethoxybenzyl)amino]-3-iodothiophene-2-carboxylate
https://huagongshe.com/reaction/2401709
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2,4-Dimethoxybenzylamine | HCID 597250 | — |
| Reactant | Ethyl 4-cyano-3-iodo-5-(methylsulfonyl)thiophene-2-carboxylate | HCID 40152062 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Ethyl 4-cyano-5-[(2,4-dimethoxybenzyl)amino]-3-iodothiophene-2-carboxylate | HCID 59250031 | 81% |
Reaction Steps
Ethyl 4-cyano-3-iodo-5-(methylsulfonyl)thiophene-2-carboxylate (5.60 g, 0.0145 mol) and 2,4-dimethoxybenzylamine (3.51 mL, 0.0234 mol) were combined in tetrahydrofuran (100 mL) and stirred at 60° C. for 3 days. The reaction was concentrated in vacuo, diluted with dichloromethane and hexanes and the resultant precipitate was filtered to yield the title compound (5.56, 81%) as a yellow solid. LCMS: (FA) ES+, 473. 1H NMR (400 MHz, d6-DMSO) δ: 9.05 (s, 1H) 7.10 (d, 1H, J=8.57 Hz), 6.60-6.50 (m, 2H), 4.30 (s, 2H), 4.22-4.14 (m, 2H), 3.80 (s, 3H), 3.75 (s, 3H), 1.26-1.21 (m, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08796268B2 |
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| Source dataset | uspto-grants-2014_08 |
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| ORD ID | ord-fa108d49bb024cc7bb3ba5dc1ae91929 |
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| Source note | uspto-grants-2014_08 |
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