Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Stannous Chloride | HCID 24479 | — |
| Reactant | HCID 58015804 | HCID 58015804 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 58016005 | HCID 58016005 | 56.8% |
Reaction Steps
To a solution of (2-chloro-5-nitro-pyrimidin-4-yl)-(1-ethyl-propyl)-amine (1 g, 4.1 mmol) in anhydrous EtOH (50 mL) is added Tin(II) chloride (2.3 g, 12.3 mmol) and concentrated HCl (1 mL) at ambient temperature. The reaction is heated to 80° C. for 1 h and quenched with 1N NaOH at 0° C. The mixture is extracted with EtOAc, washed with brine, dried over Na2SO4, and concentrated in vacuo to give 0.5 g of (2-chloro-5-amino-pyrimidin-4-yl)-(1-ethyl-propyl)-amine. The crude is used as is.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08324225B2 |
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| Source dataset | uspto-grants-2012_12 |
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| ORD ID | ord-cc779a3bcf674db990ae252581ab45cc |
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| Source note | uspto-grants-2012_12 |
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