HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1772161Generated: October 30, 2026
Dimethyl Sulfoxide → HCID 123644455, compound
https://huagongshe.com/reaction/1772161
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Potassium Acetate | HCID 517044 | — |
| Reactant | Bis(neopentyl glycolato)diboron | HCID 2734316 | — |
| Reactant | HCID 117902383 | HCID 117902383 | — |
| Catalyst | Palladium Chloride | HCID 24290 | — |
| Catalyst | Ferrocene-1,1'-bis-(diphenylphosphine) | HCID 635956 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 123644455 | HCID 123644455 | — |
Reaction Steps
1,1′-Bis(diphenylphosphino)ferrocene]dichloropalladium(II) (0.41 g, 0.6 mmol) is added to a mixture of tert-butyl-N-{1-[(6-amino-4-bromopyridin-2-yl)carbamoyl]ethyl}-N-methyl-carbamate B1 (5.2 g, 11.2 mmol), bis(neopentyl glycolato)diboron (5.1 g, 22.4 mmol), KOAc (3.3 g, 33.6 mmol) and DMSO (20 ml) under argon atmosphere and the mixture is stirred at 80° C. for 5 h. The mixture is diluted with DCM and extracted with a saturated aqueous sodium hydrogencarbonate solution. The combined organic layers are dried over MgSO4 and concentrated in vacuo. The product is purified by RP HPLC. Yield: 3.2 g (85%). HPLC-MS: M+H=339; tR=0.51 min (Method—2).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09249151B2 |
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| Source dataset | uspto-grants-2016_02 |
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| ORD ID | ord-984811661e6c492d8c8cfbbdccb2527d |
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| Source note | uspto-grants-2016_02 |
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