HuagongsheHuagongshe Chemistry Print Report · For research reference only
methyl (2S)-2-aminohexanoate hydrochloride → HCID 54529792, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | methyl (2S)-2-aminohexanoate hydrochloride | HCID 14039065 | — |
| Reactant | HCID 18380282 | HCID 18380282 | — |
| Product | HCID 54529792 | HCID 54529792 | — |
Reaction Steps
Using General Procedure G, followed by hydrolysis set forth in General Procedure C, N-(quinolin-3-yl)-D,L-alanine was prepared. This compound was then coupled to L-norleucine methyl ester hydrochloride (Sigma) using General Procedure D to provide for the title compound as an oil. The latter reaction was monitored by tlc (Rf=0.76 in 10% methanol/methylene chloride and 0.07 in 1:1 EtOAc:Hexanes and the product was purified by flash chromatography using 10% methanol/methylene chloride as the eluent.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06495693B2 |
| Source dataset | uspto-grants-2002_12 |
| ORD ID | ord-0d08bd304c224a0ba8e9d4551e692592 |
| Source note | uspto-grants-2002_12 |