HuagongsheHuagongshe Chemistry Print Report · For research reference only
2(R)-benzyl-3-(N-benzyl-N-methylaminocarbonyl)propionic acid → (2R, 4S, 5S)-5-{N-[2(R)-Benzyl-3-(N-benzyl-N-methylaminocarbonyl)propionyl]-3-(4-thiazolyl)-L-alanyl}amino-6-cyclohexyl-N-ethyl-4-hydroxy-2-methylhexanamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2(R)-benzyl-3-(N-benzyl-N-methylaminocarbonyl)propionic acid | HCID 15045754 | — |
| Reactant | (2R, 4S, 5S)-5-[N-(t-butoxycarbonyl)-3-(4-thiazolyl)-L-alanyl]amino-6-cyclohexyl-N-ethyl-4-hydroxy-2-methylhexanamide | HCID 15045769 | — |
| Product | (2R, 4S, 5S)-5-{N-[2(R)-Benzyl-3-(N-benzyl-N-methylaminocarbonyl)propionyl]-3-(4-thiazolyl)-L-alanyl}amino-6-cyclohexyl-N-ethyl-4-hydroxy-2-methylhexanamide | HCID 15045746 | 29% |
Reaction Steps
The procedure described in Example 6(b) was repeated, but using 325 mg (0.62 mmole) of (2R, 4S, 5S)-5-[N-(t-butoxycarbonyl)-3-(4-thiazolyl)-L-alanyl]amino-6-cyclohexyl-N-ethyl-4-hydroxy-2-methylhexanamide [prepared as described in Example 19(a)] and 200 mg (0.64 mmole) of 2(R)-benzyl-3-(N-benzyl-N-methylaminocarbonyl)propionic acid, to afford 129 mg of the title compound as white crystals, melting at 148°-150° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05378689 |
| Source dataset | uspto-grants-1995_01 |
| ORD ID | ord-6df18e238ae6445684d6a915b41d3dda |
| Source note | uspto-grants-1995_01 |