HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenol → 7-(Phenyloxy)-1-heptanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenol | HCID 996 | — |
| Reactant | 1-Heptanol, 7-bromo- | HCID 66284 | — |
| Reactant | Nadh | HCID 439153 | — |
| Product | 7-(Phenyloxy)-1-heptanol | HCID 15856264 | — |
Reaction Steps
In a further aspect, the invention provides a method of making a bacterial NAD synthetase inhibitor compound comprising the steps of: a. alkylating a phenol with 7-bromo-1-heptanol to provide 7-(phenyloxy)-1-heptanol; b. mesylating 7-(phenyloxy)-1-heptanol to provide 7-(phenyloxy)-1-heptyl methanesulfonate; c. esterifying 7-(phenyloxy)-1-heptyl-methanesulfonate to provide 7-(phenyloxy)-1-heptyl nicotinate; and d. n-methylating 7-(phenyloxy)-1-heptyl nicotinate to provide [7-(phenyloxy)-1-heptyl-(N-methyl)nictotinate]iodide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06727237B2 |
| Source dataset | uspto-grants-2004_04 |
| ORD ID | ord-b0a7b6120bce44a09f67f975c2c9692f |
| Source note | uspto-grants-2004_04 |