HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 525614Generated: October 29, 2026
Dichloromethane → HCID 86695502, compound
https://huagongshe.com/reaction/525614
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 2,2-difluoro-1-((4S,5R)-4-(fluoromethyl)-2,2-dimethyl-5-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)oxazolidin-3-yl)ethanone | HCID 86695414 | — |
| Reactant | benzyl N-[1-(5-bromopyridin-2-yl)ethyl]carbamate | HCID 86695503 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 86695502 | HCID 86695502 | — |
Reaction Steps
A mixture of the product of Example 22, Step 3, benzyl (1-(5-bromopyridin-2-yl)ethyl)carbamate, 2.0M sodium carbonate in water (3.1 mL, 6.2 mmol) in dioxane is degassed with nitrogen. 1,1′-bis(diphenylphosphino)ferrocene dichloropalladium(ii) complex with dichloromethane (169 mg, 0.21 mmol) is added and the mixture heated to 80° C. overnight. After cooling to room temperature the reaction mixture is diluted with water (25 mL) and extracted with ethylacetate. The organic phase is separated, dried over MgSO4, and concentrated under reduced pressure. The crude material is purified using silica chromatography eluting from 25% ethylacetate/heptane to 35% ethylacetate/heptane to give the title product (1.00 g): m/z: 541.22.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09340564B2 |
|---|
| Source dataset | uspto-grants-2016_05 |
|---|
| ORD ID | ord-f651b4d2300542fc8ec169d7e4a39f40 |
|---|
| Source note | uspto-grants-2016_05 |
|---|
