HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 250387Generated: October 27, 2026
Glycine → Glycine, N-[[4-hydroxy-7-(phenylthio)-3-isoquinolinyl]carbonyl]-
https://huagongshe.com/reaction/250387
Participants
| Role | Name | HCID | Charge |
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| Reactant | Glycine | HCID 750 | — |
| Reactant | Methanol | HCID 887 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | 4-Hydroxy-7-phenylsulfanyl-isoquinoline-3-carboxylic acid butyl ester | HCID 66713092 | — |
| Product | Glycine, N-[[4-hydroxy-7-(phenylthio)-3-isoquinolinyl]carbonyl]- | HCID 11245165 | 90.8% |
Reaction Steps
A mixture of 113 mg of 4-hydroxy-7-phenylsulfanyl-isoquinoline-3-carboxylic acid butyl ester (0.32 mmol), 244 mg of glycine (3.2 mmol), and 6.4 ml of a 0.5 N solution of sodium methoxide in methanol (3.2 mmol) was refluxed for 24 h with stirring. Then the solvent was evaporated in vacuo, the residue dissolved in 25 ml of water and the resulting solution was washed twice with 50 ml of ethyl acetate. The pH of the solution was subsequently adjusted to about 3 by addition of concentrated hydrochloric acid and the resulting slurry was extracted twice with 25 ml of ethyl acetate. The combined extracts were dried over MgSO4 and evaporated in vacuo. 103 mg of the title compound were obtained; 1H NMR (DMSO-d6): δ=9.32 (t, 1H), 8.74 (s, 1H), 8.19 (d, 1H), 7.94 (d, 1H), 7.45 to 7.65 (m, 6H), 4.02 (d, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07863292B2 |
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| Source dataset | uspto-grants-2011_01 |
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| ORD ID | ord-90fb49551c0d45a7930edc76ab99f86a |
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| Source note | uspto-grants-2011_01 |
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