HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1750679Generated: October 31, 2026
2-Ethenyl-4,4,5,5-tetramethyl-1,3,2-dioxaborolane → HCID 118308202, compound
https://huagongshe.com/reaction/1750679
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Ethenyl-4,4,5,5-tetramethyl-1,3,2-dioxaborolane | HCID 5233012 | — |
| Reactant | HCID 118308077 | HCID 118308077 | — |
| Reactant | HCID 118308312 | HCID 118308312 | — |
| Reactant | HCID 118308320 | HCID 118308320 | — |
| Product | HCID 118308202 | HCID 118308202 | — |
Reaction Steps
Prepared according to the procedure for N-[(1S,2S)-2-[(5-cyclopropylpyrazin-2-yl)amino]cyclopentyl]-2-(2H-1,2,3-triazol-2-yl)benzamide (Example 112) from N-[(1S,2S)-2-[(5-bromopyrazin-2-yl)amino]cyclopentyl]-2-(2H-1,2,3-triazol-2-yl)benzamide and N-[(1S,2S)-2-[(5-chloropyrazin-2-yl)amino]cyclopentyl]-2-(2H-1,2,3-triazol-2-yl)benzamide (Intermediate 30a and 30b; 100 mg, 0.23 mmol) and 2-ethenyl-4,4,5,5-tetramethyl-1,3,2-dioxaborolane (CAS number 75927-49-0; 151 mg, 0.98 mmol) except this was purified only by column chromatography (silica, 0-100% ethyl acetate/petrol) and then was dissolved in ethanol (1.4 ml). To this was then added palladium on carbon (10% wt, 50% wet) (15 mg, 0.014 mmol) and the resulting mixture was stirred under a balloon of hydrogen gas for 2 hours. The reaction was filtered through diatomaceous earth (commercially sold under the trade mark “Celite”) and concentrated in vacuo. This was purified by column chromatography (basic silica, 0-100% ethyl acetate/petrol) to afford the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09156829B2 |
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| Source dataset | uspto-grants-2015_10 |
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| ORD ID | ord-422fb477d24645f289c0342590696a62 |
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| Source note | uspto-grants-2015_10 |
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