HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1661079Generated: October 27, 2026
Sodium Iodide → 1-(4-(5-Chloro-2,3-dihydrospiro[indene-1,3'-pyrrolidine]-1'-yl)butyl)-5-(thiophen-2-yl)pyrimidine-2,4(1h,3h)-dione hydrochloride
https://huagongshe.com/reaction/1661079
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1-(4-chlorobutyl)-5-(thiophen-2-yl)pyrimidine-2,4(1H,3H)-dione | HCID 59233926 | — |
| Reactant | 5-Chloro-2,3-dihydrospiro[indene-1,3'-pyrrolidine] hydrochloride | HCID 67427992 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Product | 1-(4-(5-Chloro-2,3-dihydrospiro[indene-1,3'-pyrrolidine]-1'-yl)butyl)-5-(thiophen-2-yl)pyrimidine-2,4(1h,3h)-dione hydrochloride | HCID 67428567 | 81.2% |
Reaction Steps
A mixture of 1-(4-chlorobutyl)-5-(thiophen-2-yl)pyrimidine-2,4(1H,3H)-dione (Prep23, 50 mg, 0.18 mmol), 5-chloro-2,3-dihydrospiro[indene-1,3′-pyrrolidine]hydrochloride (Prep10, 66 mg, 0.27 mmol), potassium carbonate (112 mg, 0.81 mmol), sodium iodide (108 mg, 0.72 mmol) and NMP (1 ml) was stirred at 70° C. overnight. Then it was cooled down to room temperature and diluted with water and extracted with ethyl acetate. The EA phase was evaporated and the crude purified by preparative TLC (TLC analysis performed by eluting with EA) to give the free base of the title compound (72 mg). The compound was purified by preparative HPLC and treated with a 1N solution of HCl-ether and freeze-dried give the title compound (51 mg, y=58%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08030322B2 |
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| Source dataset | uspto-grants-2011_10 |
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| ORD ID | ord-e6696fba71d84ab3bbff136e7b725cff |
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| Source note | uspto-grants-2011_10 |
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