HuagongsheHuagongshe Chemistry Print Report · For research reference only
2(R)-(4-Methoxybenzyl)-3-(morpholinocarbonyl)propionic acid → (2R, 4S, 5S)-N-Butyl-6-cyclohexyl-4-hydroxy-5-{N-[2(R)-(4-methoxybenzyl)-3-(morpholinocarbonyl)propionyl]-3-(4-thiazolyl)-L-alanyl}amino-2-methylhexanamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2(R)-(4-Methoxybenzyl)-3-(morpholinocarbonyl)propionic acid | HCID 14429473 | — |
| Reactant | (2R, 4S, 5S)-5-[N-(t-butoxycarbonyl)-3-(4-thiazolyl)-L-alanyl]amino-N-butyl-6-cyclohexyl-4-hydroxy-2-methylhexanamide | HCID 15045764 | — |
| Product | (2R, 4S, 5S)-N-Butyl-6-cyclohexyl-4-hydroxy-5-{N-[2(R)-(4-methoxybenzyl)-3-(morpholinocarbonyl)propionyl]-3-(4-thiazolyl)-L-alanyl}amino-2-methylhexanamide | HCID 15045735 | 59.2% |
Reaction Steps
The procedure described in Example 6(b) was repeated, but using 200 mg (0.36 mmole) of (2R, 4S, 5S)-5-[N-(t-butoxycarbonyl)-3-(4-thiazolyl)-L-alanyl]amino-N-butyl-6-cyclohexyl-4-hydroxy-2-methylhexanamide [prepared as described in Example 6(a)] and 110 mg (0.36 mmole) of 2(R)-(4-methoxybenzyl)-3-(morpholinocarbonyl)propionic acid, to afford 158 mg of the title compound as a white powder, melting at 130°-132° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05378689 |
| Source dataset | uspto-grants-1995_01 |
| ORD ID | ord-40eaecc72a1d45dc9721706ec5a1fc78 |
| Source note | uspto-grants-1995_01 |