HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 730354Generated: October 30, 2026
HCID 86604765, compound → HCID 67278012, compound
https://huagongshe.com/reaction/730354
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 86604765 | HCID 86604765 | — |
| Reactant | HCID 178418573 | HCID 178418573 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 67278012 | HCID 67278012 | — |
Reaction Steps
To a solution of crude (4R)-4-[({3-chloro-4-[(1-methylethyl)oxy]phenyl}carbonyl)amino]-5-[4-(1-methyl-2-{[methyl(methyloxy)amino]carbonyl}-1H-imidazol-4-yl)phenyl]pentanoic acid (3.18 mmol) in anhydrous THF (16 mL) under nitrogen at 0° C. was added methylmagnesium bromide (10.6 mL, 10 equiv, 3.0 M in ether) dropwise by syringe. The reaction was stirred for 30 minutes at 0° C. and then carefully quenched with sat. aq. NH4Cl solution (10 ML), followed by 1 N HCl solution (60 mL) such that the pH of the aqueous layer ˜5.5. The product was extracted with EtOAc (4×40 mL) and the combined organic layers were dried over MgSO4 and concentrated in vacuo to give the title compound, which was used directly in the next reaction. ESMS [M+H]+=512.4.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07582668B2 |
|---|
| Source dataset | uspto-grants-2009_09 |
|---|
| ORD ID | ord-3cf40cf0e81a409db19c772d9fdd7727 |
|---|
| Source note | uspto-grants-2009_09 |
|---|