HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2217331Generated: October 29, 2026
Diisopropylethylamine → HCID 11514839, compound
https://huagongshe.com/reaction/2217331
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 3-Pyridinecarbonyl chloride, hydrochloride (1:1) | HCID 88438 | — |
| Reactant | HCID 49796119 | HCID 49796119 | — |
| Solvent | 1,1-Dichloroethane | HCID 6365 | — |
| Product | HCID 11514839 | HCID 11514839 | — |
Reaction Steps
A suspension of 8H-Indeno[1,2-d]thiazol-2-ylamine hydroiodide 1a (Prepared in Example 1, Step 1, mg; mmol), nicotinoyl chloride hydrochloride (92 mg; 0.50 mmol) and diisopropylethylamine (0.50 mL; 2.77 mmol) in dichloroethane was heated in a sealed tube to 120° C. in a microwave oven for 10 minutes. The mixture was allowed to cool to room temperature and the solvent removed in vacuo. The residue was taken up into 2 M sodium carbonate solution and extracted with ethyl acetate. The extracts were dried (sodium sulfate), filtered and concentrated in vacuo. The crude product was chromatographed on silica gel (eluent=50% ethyl acetate/hexanes to 100% ethyl acetate/hexanes gradient) to provide 43 mg of N-(8H-Indeno[1,2-d]thiazol-2-yl)-nicotinamide 7. EI-HRMS m/e calcd for C16H11N4OS (M+) 293.0623, found 293.0620.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07407977B2 |
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| Source dataset | uspto-grants-2008_08 |
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| ORD ID | ord-2974063c7a2f4a8c90b33e077f51e383 |
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| Source note | uspto-grants-2008_08 |
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