HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 882969Generated: October 25, 2026
Sodium Iodide → 1-(2-Amino-4,6-dichloropyrimidin-5-yl)-3-buten-1-ol
https://huagongshe.com/reaction/882969
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | 2-Amino-4,6-dichloropyrimidine-5-carboxaldehyde | HCID 265546 | — |
| Reactant | Indium | HCID 5359967 | — |
| Catalyst | Zinc | HCID 23994 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-(2-Amino-4,6-dichloropyrimidin-5-yl)-3-buten-1-ol | HCID 58201189 | — |
Reaction Steps
Indium powder (0.23 g) and zinc powder (1.31 g) were added to a mixture composed of commercially available 2-amino-4,6-dichloropyrimidine-5-carboaldehyde (1.92 g) and N,N-dimethylformamide (20 ml). Thereafter, sodium iodide (0.15 g) and allyl bromide (1.73 ml) were added to the mixture at room temperature. The resulting mixture was stirred for 3 hours. Thereafter, the reaction mixture was filtered through celite, and ethyl acetate was then added to the filtrate. The resulting mixture was successively washed with 1 N hydrochloric acid and a saturated saline in this order. The organic layer was dried over anhydrous sodium sulfate, and was then concentrated. Thereafter, hexane was added to the residue, and a precipitate was then collected by filtration, so as to obtain the above title compound (1.75 g) as a solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08236813B2 |
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| Source dataset | uspto-grants-2012_08 |
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| ORD ID | ord-8a2e9076b13c4b17a33388d5e1205058 |
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| Source note | uspto-grants-2012_08 |
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