HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 910302Generated: October 26, 2026
Dimethylformamide → 1-(6-Bromopyrid-2-yl)-1-methyl-3-heptylurea
https://huagongshe.com/reaction/910302
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | 1-Heptanamine | HCID 8127 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 4-Nitrophenyl chloroformate | HCID 82129 | — |
| Reactant | 6-bromo-N-methylpyridin-2-amine | HCID 13470315 | — |
| Product | 1-(6-Bromopyrid-2-yl)-1-methyl-3-heptylurea | HCID 86018868 | 80% |
Reaction Steps
1 g (5.35 mmol) of (6-bromopyrid-2-yl)-N-methylamine, 1 ml of diisopropylethylamine and 1.6 g (8 mmol) of 4-nitrophenyl chloroformate are heated at 130° C. for 15 minutes by microwave. 1.2 ml (8 mmol) of heptylamine and 7 ml of dimethylformamide are added and the reaction medium is heated at 130° C. for a further 5 minutes. The residue obtained is purified by thin-layer chromatography on silica eluted with a 70/30 heptane/ethyl acetate mixture. 1.4 g (80%) of 1-(6-bromopyrid-2-yl)-3-heptyl-1-methylurea are obtained in the form of a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08022079B2 |
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| Source dataset | uspto-grants-2011_09 |
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| ORD ID | ord-1f7d368140774a5a847e092af390a317 |
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| Source note | uspto-grants-2011_09 |
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