HuagongsheHuagongshe Chemistry Print Report · For research reference only
Boc-L-methionine → HCID 11092070, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Boc-L-methionine | HCID 89857 | — |
| Reactant | N-(tert-Butyloxycarbonyl)-D-methionine | HCID 111051 | — |
| Reactant | HCID 11033897 | HCID 11033897 | — |
| Reactant | HCID 18433619 | HCID 18433619 | — |
| Product | HCID 11092070 | HCID 11092070 | — |
Reaction Steps
Following the procedures described in Example 24, Steps F-H, but using 2-(3-tert-butyldimethylsilyloxyphenyl)aniline rather than 1-amino-4-bromo-7-(tert-butyldimethylsilyloxy)naphthalene hydrochloride, and (S)-N-(tert-butoxycarbonyl) methionine rather than (R)-N-(tert-butoxycarbonyl)methionine, the above-titled compound was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06441017B1 |
| Source dataset | uspto-grants-2002_08 |
| ORD ID | ord-64893beb84704bd58ff30b3a1d56b239 |
| Source note | uspto-grants-2002_08 |