Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Thiophenol | HCID 7969 | — |
| Reactant | HCID 178418725 | HCID 178418725 | — |
| Solvent | 1-Butanol | HCID 263 | — |
| Product | 736142-84-0 | HCID 11481564 | 92% |
Reaction Steps
To a solution of 4-chloro-1H-pyrrolo[2,3-d]pyrimidine (1.69 g, 11.0 mmol) and TEA (4.60 mL, 33.0 mmol) in 1-butanol (25.0 mL) was added benzenethiol (3.39 mL, 33.0 mmol), and the mixture was refluxed at 140° C. overnight. The reaction was then cooled to rt and concentrated in vacuo. The off-white solid was purified by silica gel chromatography eluting with a gradient of 0 to 35% EtOAc in DCM to afford the product (2.29 g, 92%). LC/MS: Rt=1.55 min, ES+ 228 (FA standard).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08207177B2 |
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| Source dataset | uspto-grants-2012_06 |
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| ORD ID | ord-632fa112846e48f29b4e0c20a300ab5f |
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| Source note | uspto-grants-2012_06 |
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