HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diazomethane → HCID 25119717, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diazomethane | HCID 9550 | — |
| Reactant | HCID 25119712 | HCID 25119712 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 25119717 | HCID 25119717 | — |
Reaction Steps
To a solution of (1R,2R)-2-{[3-({cyclopropyl[((3R,4S)-4-{4-[2-(2,6-dichloro-4-methylphenoxy)ethoxy]phenyl}piperidin-3-yl)carbonyl]amino}methyl)-5-(3-methoxypropyl)phenoxy]methyl}cyclopropanecarboxylic acid (1 eq., neutral form) from Example 2 was added a solution of diazomethane in ether until a faint yellow color persisted. The solvent was evaporated by a stream of nitrogen gas. The residue was purified by flash column chromatography (SiO2, 10% MeOH in DCM plus 1% aqueous NH4OH) afford the title compound as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08343968B2 |
| Source dataset | uspto-grants-2013_01 |
| ORD ID | ord-bd7c93d5a9af43ea9182d90a5a410840 |
| Source note | uspto-grants-2013_01 |