HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzylamine → N-(4-[(7-Methoxyheptyl)oxy]butanoyl)-L-isoleucine, ethyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzylamine | HCID 7504 | — |
| Reactant | L-Isoleucine, ethyl ester | HCID 6602175 | — |
| Reactant | 4-[(7-Methoxyheptyl)oxy]butanoyl chloride | HCID 15383030 | — |
| Reactant | 12-Methoxydodecanoyl chloride | HCID 19611759 | — |
| Reactant | L-isoleucine ethyl ester trifluoroacetate | HCID 88304807 | — |
| Product | N-(4-[(7-Methoxyheptyl)oxy]butanoyl)-L-isoleucine, ethyl ester | HCID 131721076 | — |
Reaction Steps
The title compound is prepared by the method of Example 14 using L-isoleucine ethyl ester trifluoroacetate [the title product of Example 44] as a reactant instead of benzylamine, and using an equivalent amount of 4-[(7-methoxyheptyl)oxy]butanoyl chloride [the title product of Example 100] instead of 12-methoxy-1-docecanoyl chloride [the title product of Example 11].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05929110 |
| Source dataset | uspto-grants-1999_07 |
| ORD ID | ord-238153ed43874c6e931778d9f14a122f |
| Source note | uspto-grants-1999_07 |