HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 902038Generated: October 30, 2026
Triisopropyl borate → HCID 10382614, compound
https://huagongshe.com/reaction/902038
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triisopropyl borate | HCID 21531 | — |
| Reactant | 2,2,2-trifluoro-N-(6-iodoimidazo[1,2-a]pyridin-2-yl)acetamide | HCID 11013678 | — |
| Reactant | HCID 59700618 | HCID 59700618 | — |
| Reactant | HCID 178418306 | HCID 178418306 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 10382614 | HCID 10382614 | — |
Reaction Steps
Stir 3-bromo-2-(6-methyl-pyridin-2-yl)-pyrazolo[1,5-a]pyridine (500 mg, 1.74 mmol) in THF (20 ml) at −60° C. and add t-butyl lithium (4 ml, 6.94 mmol, 1.7M in pentane). Stir for 1 hour, then add tri-isopropyl borate (1.2 ml, 5.2 mmol) and warm to 0° C. for 1 hour. Quench with 1M HCl (5 ml). Concentrate in vacuo and redissolve in a 2:1 toluene/methanol mixture (30 ml). Adjust to pH 8 with aqueous 2M Na2CO3. Add 100 mg Pd(PPh3)4 and 2,2,2-trifluoro-N-(6-iodo-imidazo[1,2-a]pyridin-2-yl)-acetamide (200 mg, 563 mmol) and heat to 90° C. for 18 hours. Acidify with 1M HCl and extract with ethyl acetate (3×100 ml). Neutralize aqueous layer with 5N NaOH and extract with ethyl acetate (3×100 ml). Concentrate organic layer in vacuo and purify on Silica gel (eluting with 70/30 Hexane/EtOAc). MS ES+ m/e 341.1 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07365066B2 |
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| Source dataset | uspto-grants-2008_04 |
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| ORD ID | ord-5ab9ddcb309e4828bdfbf2c6bc65916b |
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| Source note | uspto-grants-2008_04 |
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