HuagongsheHuagongshe Chemistry Print Report · For research reference only
tert-butyl N-methyl-N-(3-oxopropyl)carbamate → 1-{2-[{6-[(2-{3-([tert-Butoxycarbonyl)(methyl)amino]propyl}-1,2,3,4-tetrahydroisoquinolin-6-yl)amino]hexanoyl}(methyl)amino]ethyl}piperidin-4-yl biphenyl-2-ylcarbamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | tert-butyl N-methyl-N-(3-oxopropyl)carbamate | HCID 10442454 | — |
| Reactant | 1-(2-{Methyl[6-(1,2,3,4-tetrahydroisoquinolin-6-ylamino)hexanoyl]amino}ethyl)piperidin-4-yl biphenyl-2-ylcarbamate | HCID 66671813 | — |
| Product | 1-{2-[{6-[(2-{3-([tert-Butoxycarbonyl)(methyl)amino]propyl}-1,2,3,4-tetrahydroisoquinolin-6-yl)amino]hexanoyl}(methyl)amino]ethyl}piperidin-4-yl biphenyl-2-ylcarbamate | HCID 66671365 | 79.4% |
Reaction Steps
The compound (47 mg, 78.6 μmol) obtained in Example 63b and tert-butyl methyl(3-oxopropyl)carbamate (Bioorg. Med. Chem., 12, 19, 2004, 5147-5160) (18 mg, 94.3 μmol) were used to give the title compound (48 mg; yield, 79%) as a colorless oily substance 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-88038a6736044a3f8e5f9e388f50af37 |
| Source note | uspto-grants-2013_07 |