HuagongsheHuagongshe Chemistry Print Report · For research reference only
ethyl 4-{N-[4-(2-tetrahydropyranyloxy)nonyl]methanesulfonamido}butoxyacetate → 7-[N-(4(R)-hydroxy-2-nonynyl)methanesulfonamido]heptanoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | ethyl 4-{N-[4-(2-tetrahydropyranyloxy)nonyl]methanesulfonamido}butoxyacetate | HCID 20327707 | — |
| Reactant | Ethyl 2-(4-bromobutoxy)acetate | HCID 20436843 | — |
| Reactant | Ethyl 7-bromo-2-methylheptanoate | HCID 22770549 | — |
| Product | 7-[N-(4(R)-hydroxy-2-nonynyl)methanesulfonamido]heptanoic acid | HCID 22798404 | — |
Reaction Steps
The synthesis of this compound is carried out as described in Example 8 except that, in Step A, the ethyl 7-bromo-2-methylheptanoate is replaced by an equimolar amount of ethyl 4-bromobutoxyacetate (Example M). The product of Step A is thus ethyl 4-{N-[4-(2-tetrahydropyranyloxy)nonyl]methanesulfonamido}butoxyacetate. The subsequent step yields 4-[N-(4-hydroxynonyl)methanesulfonamido]butoxyacetic acid (B).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04033996 |
| Source dataset | uspto-grants-1977_07 |
| ORD ID | ord-0a20112412f746a780939a517870c513 |
| Source note | uspto-grants-1977_07 |