HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2215496Generated: October 27, 2026
Phenyl Methylcarbamate → HCID 21054849, compound
https://huagongshe.com/reaction/2215496
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phenyl Methylcarbamate | HCID 16034 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 5-(6-Amino-pyrimidin-4-yloxy)-1H-indole | HCID 21949266 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 21054849 | HCID 21054849 | 63.2% |
Reaction Steps
Sodium hydride (199 mg, 4.97 mmol) was suspended in N,N-dimethylformamide (10 ml) under nitrogen atmosphere, 6-(1H-indol-5-yloxy)pyrimidin-4-ylamine (1.07 g, 4.73 mmol) synthesized in Production example 2-2 was gradually added while the reaction mixture was stirred at room temperature. After 30 minutes, the reaction mixture was cooled with an ice water bath, then phenyl N-methylcarbamate (751 mg, 4.97 mmol) synthesized in Production example 2-1 was added. The reaction mixture was heated to room temperature and stirred for 1 hour. The reaction mixture was partitioned between ethyl acetate and water. The organic layer was washed with water and brine, and was dried over anhydrous magnesium sulfate. After the solvent was distilled off, the residue was purified by silica gel column chromatography (eluent; ethyl acetate) to yield the title compound (847 mg, 2.99 mmol, 63%) as white crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07109219B2 |
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| Source dataset | uspto-grants-2006_09 |
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| ORD ID | ord-d40e5e92863a4e88abca819a5d607300 |
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| Source note | uspto-grants-2006_09 |
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