HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1728213Generated: November 1, 2026
HCID 68963574, compound → HCID 57566077, compound
https://huagongshe.com/reaction/1728213
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 68963574 | HCID 68963574 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Trifluoroacetic acid | HCID 6422 | — |
| Product | HCID 57566077 | HCID 57566077 | 50% |
Reaction Steps
The chiral (2′R,3R,4′S)-1′-(aminocarbonyl-methyl)-6-bromo-4′-(3-chlorophenyl)-2′-(1-methyl cyclopropyl)-2,3-dihydro-2,6′-dioxospiro[indole-3,3′-piperidine]-1-methoxyethyl trimethylsilane (25 mg, 0.039 mmol) was dissolved in a solution of trifluoroacetic acid (2 mL) in dichloromethane (5 mL). The reaction mixture was stirred at room temperature for 0.5 h, then concentrated. The residue was dissolved in a solution of methanol (3 mL) and N,N′-diisopropylethylamine (1 mL). The reaction tube was then placed into the cavity of a focused monomode microwave reactor and the contents of the flask were irradiated at 120° C. for 30 min. The reaction mixture was concentrated and the residue was purified by Prep-HPLC to give title compound (10 mg, 50%) m/z (M+H)+: 516
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07495007B2 |
|---|
| Source dataset | uspto-grants-2009_02 |
|---|
| ORD ID | ord-f1c84b516f33415a9503ff0bfdd201cd |
|---|
| Source note | uspto-grants-2009_02 |
|---|