HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1428495Generated: October 26, 2026
Diisopropylethylamine → HCID 57470420, compound
https://huagongshe.com/reaction/1428495
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 3H-spiro(2-benzofuran-1,4'-piperidine) hydrochloride | HCID 22509330 | — |
| Reactant | 2,3-Dichloro-4-iodopyridine | HCID 44887038 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 57470420 | HCID 57470420 | — |
Reaction Steps
A mixture of D10 (1 g, 3.655 mmol), spiro[isobenzofuran-1(3H),4′-piperidine], hydrochloride [CAS 37663-44-8] (0.83 g, 4.386 mmol) and DIPEA (1.273 ml, 7.309 mmol) in CH3CN (9 ml) was heated in a sealed tube at 110° C. for 16 h. The mixture was then treated with NaHCO3 (aqueous sat. solution) and extrated with EtOAc. The organic layer was separated, dried (Na2SO4) and concentrated in vacuo. The crude product was purified by column chromatography (silica gel; DCM/EtOAc up to 2% as eluent). The desired fractions were collected and concentrated in vacuo to yield intermediate compound D21 (0.199 g, 16%) as a white solid. M.P. 160.8° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08937060B2 |
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| Source dataset | uspto-grants-2015_01 |
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| ORD ID | ord-3aa85b37702f416e9a4a6914f68f2a81 |
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| Source note | uspto-grants-2015_01 |
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