HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloride methanol → 1-{2-[Methyl(6-{[4-(piperazin-1-ylcarbonyl)phenyl]amino}hexanoyl)amino]ethyl}piperidin-4-yl biphenyl-2-ylcarbamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloride methanol | HCID 21893726 | — |
| Reactant | tert-Butyl 4-{[4-({6-[(2-{4-[(biphenyl-2-ylcarbamoyl)oxy]piperidin-1-yl}ethyl)(methyl)amino]-6-oxohexyl}amino)phenyl]carbonyl}piperazine-1-carboxylate | HCID 86761917 | — |
| Product | 1-{2-[Methyl(6-{[4-(piperazin-1-ylcarbonyl)phenyl]amino}hexanoyl)amino]ethyl}piperidin-4-yl biphenyl-2-ylcarbamate | HCID 66671480 | 78% |
Reaction Steps
The compound (98 mg, 0.130 mmol) obtained in Example 92a and 2 N hydrochloric acid-methanol (1.30 mL, 2.60 mmol) were used to give the title compound (66 mg; yield, 78%) as a white solid according to the method described in Example 89e.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08476253B2 |
| Source dataset | uspto-grants-2013_07 |
| ORD ID | ord-9ed3d77511c14eff9c8d381eba808be7 |
| Source note | uspto-grants-2013_07 |