HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1800732Generated: October 30, 2026
Sodium Bicarbonate → HCID 59507053, compound
https://huagongshe.com/reaction/1800732
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 5-(propan-2-yl)-1H-pyrazole-3-carboxylic acid | HCID 776421 | — |
| Reactant | Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1) | HCID 9886157 | — |
| Reactant | N-{3-[(2-amino[1,3]thiazolo[5,4-d]pyrimidin-5-yl)amino]-4-methylphenyl}-3-(1-cyano-1-methylethyl)benzamide | HCID 86646090 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 59507053 | HCID 59507053 | 32% |
Reaction Steps
To a solution of N-{3-[(2-amino[1,3]thiazolo[5,4-d]pyrimidin-5-yl)amino]-4-methylphenyl}-3-(1-cyano-1-methylethyl)benzamide (82 mg, 185 μmol) produced in Example D25(iii) in pyridine (3 mL) were added 5-(1-methylethyl)-1H-pyrazole-3-carboxylic acid (57 mg, 370 μmol) and O-(7-azabenzotriazol-1-yl)-N,N,N′,N′-tetramethyluronium hexafluorophosphate (211 mg, 555 μmol), and the mixture was stirred at 90° C. for 21 hr. To the reaction mixture was added saturated aqueous sodium hydrogen carbonate solution (15 mL), and the mixture was extracted with ethyl acetate (20 mL, 5 mL). The combined organic layer was washed with saturated brine (5 mL), and dried over anhydrous sodium sulfate. The insoluble material was filtered off, and the filtrate was concentrated under reduced pressure. The obtained residue was purified by basic silica gel column chromatography (ethyl acetate/methanol=100/0→92/8), and the fractions containing the object product were concentrated under reduced pressure. The obtained residue was recrystallized from N,N-dimethylformamide and diethyl ether to give the title compound (34 mg, 32%) as pale-yellow crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08344135B2 |
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| Source dataset | uspto-grants-2013_01 |
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| ORD ID | ord-956ef2eb3edf4a6996886d8b278396a3 |
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| Source note | uspto-grants-2013_01 |
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