Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Glycine | HCID 750 | — |
| Reactant | Sodium methanolate methanol | HCID 23694274 | — |
| Reactant | HCID 68426549 | HCID 68426549 | — |
| Product | HCID 24757158 | HCID 24757158 | 54.6% |
Reaction Steps
A mixture of 7-hydroxy-2-phenoxy-thiazolo[4,5-c]pyridine-6-carboxylic acid ethyl ester (81 mg, 0.26 mmol) and glycine (386 mg, 5.14 mmol) in 0.5 M sodium methoxide/methanol (9.8 mL, 4.88 mmol) was refluxed for 3 days before it was cooled to room temperature and concentrated in vacuo. The residue was dissolved in water and extracted with dichloromethane. The remaining aqueous layer was acidified to pH=3 with 1N HCl (7.3 mL). The suspension was extracted with ethyl acetate. The organic layer was dried over sodium sulfate, concentrated in vacuo and purified on a C18 reverse column with a gradient of 0.1% TFA in water and 0.1% TFA in acetonitrile to give the title compound as a brown solid (49 mg): 1H NMR (DMSO-d6, 200 MHz): δ=13.16 (s, 1H), 9.39 (br s, 1H), 8.60 (s, 1H), 7.55 (m, 4H), 7.42 (m, 1H), 4.01 (d, J=6.4 Hz, 2H); MS: (+) m/z 346.00 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07696223B2 |
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| Source dataset | uspto-grants-2010_04 |
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| ORD ID | ord-812ec982c61c4c4f86d2d667c6554b9d |
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| Source note | uspto-grants-2010_04 |
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