HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-(Methylamino)propanoic acid, N-BOC protected → Benzyl {6-[(2-{4-[(biphenyl-2-ylcarbamoyl)oxy]piperidin-1-yl}ethyl)(methyl)amino]-6-oxohexyl}(4-{[N-(tert-butoxycarbonyl)-N-methyl-beta-alanyl](methyl)amino}phenyl)carbamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-(Methylamino)propanoic acid, N-BOC protected | HCID 2760952 | — |
| Reactant | Benzyl {6-[(2-{4-[(biphenyl-2-ylcarbamoyl)oxy]piperidin-1-yl}ethyl)(methyl)amino]-6-oxohexyl}[4-(methylamino)phenyl]carbamate | HCID 66671650 | — |
| Product | Benzyl {6-[(2-{4-[(biphenyl-2-ylcarbamoyl)oxy]piperidin-1-yl}ethyl)(methyl)amino]-6-oxohexyl}(4-{[N-(tert-butoxycarbonyl)-N-methyl-beta-alanyl](methyl)amino}phenyl)carbamate | HCID 66793891 | 112.2% |
Reaction Steps
N-(tert-Butoxycarbonyl)-N-methyl-β-alanine (41 mg, 0.19 mmol) and the compound (150 mg, 0.21 mmol) obtained in Example 97c were used to give the title compound (190 mg; yield, 100%) as a white solid according to the method described in Example 41a.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08476253B2 |
| Source dataset | uspto-grants-2013_07 |
| ORD ID | ord-12c2398d6613446e8a7cfb7e548cb84f |
| Source note | uspto-grants-2013_07 |