HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1371391Generated: November 1, 2026
Pyrrolidine → 2-[3-(pyrrolidin-1-ylsulfonyl)propyl]-1H-isoindole-1,3(2H)-dione
https://huagongshe.com/reaction/1371391
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pyrrolidine | HCID 31268 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 3-(1,3-dioxo-2,3-dihydro-1H-isoindol-2-yl)propane-1-sulfonyl chloride | HCID 15453270 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-[3-(pyrrolidin-1-ylsulfonyl)propyl]-1H-isoindole-1,3(2H)-dione | HCID 23089228 | — |
Reaction Steps
A solution of 3-(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)propane-1-sulfonyl chloride (0.288 g) in dry tetrahydrofuran (5 ml) was treated with N,N-diisopropylethylamine (0.350 ml) and pyrrolidine (0.10 ml) at 22° C. under nitrogen, and the mixture was stirred at 22° C. for 1 h. After standing overnight at room temperature, the mixture was partitioned between saturated aqueous sodium bicarbonate (10 ml) and ethyl acetate (2×10 ml). The organic layers were washed with brine, dried (MgSO4) and evaporated in vacuo to give a white solid (0.145 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07157457B2 |
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| Source dataset | uspto-grants-2007_01 |
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| ORD ID | ord-ba8c723901e04e50846e4c072c9b295c |
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| Source note | uspto-grants-2007_01 |
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