HuagongsheHuagongshe Chemistry Print Report · For research reference only
L-Alanine → 2-(S)-[(4-Hydroxy-7-phenylsulfanyl-isoquinoline-3-carbonyl)-amino]-propionic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | L-Alanine | HCID 5950 | — |
| Reactant | 4-Hydroxy-7-phenylsulfanyl-isoquinoline-3-carboxylic acid butyl ester | HCID 66713092 | — |
| Solvent | Sodium methanolate methanol | HCID 23694274 | — |
| Product | 2-(S)-[(4-Hydroxy-7-phenylsulfanyl-isoquinoline-3-carbonyl)-amino]-propionic acid | HCID 24861740 | 72% |
Reaction Steps
A mixture of 4-hydroxy-7-phenylsulfanyl-isoquinoline-3-carboxylic acid butyl ester (0.20 g) and L-alanine (0.75 g) in 0.5 M NaOMe/MeOH (11.3 ml) was heated to reflux for 36 h. After cooling, reaction mixture was concentrated. The residue was suspended in water (50 ml) and extracted with ethyl acetate (50 ml) which was discarded. The aqueous layer was acidified by 2 N HCl aqueous solution. Extracted with ethyl acetate (2×50 ml). Combined organic layers were dried over magnesium sulfate, filtered, and concentrated to give the title compound (0.15 g). MS-(−)-ion: M−1=367.1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07863292B2 |
| Source dataset | uspto-grants-2011_01 |
| ORD ID | ord-33eeda3e99a348778876622894aff96f |
| Source note | uspto-grants-2011_01 |