HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1788034Generated: October 29, 2026
Sodium Iodide → {2-[4-(4-Chlorophenyl)piperazin-1-yl]-7-methoxythieno[3,2-d]pyrimidin-4-yl}propylamine
https://huagongshe.com/reaction/1788034
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | {7-Bromo-2-[4-(4-chlorophenyl)piperazin-1-yl]thieno[3,2-d]pyrimidin-4-yl}propylamine | HCID 86616283 | — |
| Catalyst | Copper oxide | HCID 14829 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | {2-[4-(4-Chlorophenyl)piperazin-1-yl]-7-methoxythieno[3,2-d]pyrimidin-4-yl}propylamine | HCID 86616284 | 20% |
Reaction Steps
2.00 g (4.28 mmol) of {7-bromo-2-[4-(4-chlorophenyl)piperazin-1-yl]thieno[3,2-d]pyrimidin-4-yl}propylamine (VII) is placed in 15 mL of methanol and cooled to some extent. First 0.995 g (18.42 mmol) of sodium methoxide, then 0.187 g (2.36 mmol) of copper (II) oxide, and 0.040 g (0.27 mmol) of sodium iodide are added. The reaction mixture is heated to 160° C. in the microwave for 0.75 hours. Then it is suction filtered through silica gel and the mother liquor is concentrated by evaporation. The residue is dissolved and any insoluble matter is removed by suction filtering. Further purification is carried out by preparative HPLC. 0.23 g of product VIII (20%) is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07511045B2 |
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| Source dataset | uspto-grants-2009_03 |
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| ORD ID | ord-c7cd7bb8a1c444668c417583027e39d9 |
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| Source note | uspto-grants-2009_03 |
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