HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1615861Generated: November 3, 2026
Diisopropylethylamine → HCID 66865455, compound
https://huagongshe.com/reaction/1615861
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 58118678 | HCID 58118678 | — |
| Reactant | HCID 86650290 | HCID 86650290 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 66865455 | HCID 66865455 | — |
Reaction Steps
A mixture of tert-butyl (8R)-8-(3,5-difluorophenyl)-8-methyl-10-oxo-9-[2-oxo-2-(pentafluorophenoxy)ethyl]-6,9-diazaspiro[4.5]decane-6-carboxylate from Step A (119 mg, 0.197 mmol), (2R)-5-hydroxy-1′-{[2-(trimethylsilyl)ethoxy]methyl}-1,3-dihydrospiro[indene-2,3′-pyrrolo[2,3-b]pyridin]-2′(1′H)-one (77 mg, 0.201 mmol, described in Intermediate 35), and N,N-diisopropylethylamine (0.17 mL, 0.98 mmol) in DMF (0.5 mL) was heated at 150° C. in a microwave reactor for 30 min. The reaction mixture was cooled and partitioned between saturated aqueous NaHCO3 (20 mL) and EtOAc (30 mL). The organic layer was dried over Na2SO4, filtered, and concentrated in vacuo. The crude product was purified on silica gel, eluting with a gradient of hexanes:EtOAc—100:0 to 0:100, to provide the title compound. MS: m/z=803.7 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08765759B2 |
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| Source dataset | uspto-grants-2014_07 |
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| ORD ID | ord-8b8913e8cb8f4bdcb4ae5dbd3d0aa477 |
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| Source note | uspto-grants-2014_07 |
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