Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Methanol | HCID 887 | — |
| Reactant | HCID 21949160 | HCID 21949160 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 21949139 | HCID 21949139 | 82% |
Reaction Steps
A 7N methanol solution of ammonia (50 ml) and tetrahydrofuran (20 ml) were added to 6-chloro-4-(1H-4-indolylamino)pyrimidine (599 mg, 2.5 mmol) and the reaction mixture was heated in a sealed tube at 130° C. for 137 hours. The solvent was distilled off under reduced pressure; the residue was purified by silica gel column chromatography (eluent; ethyl acetate:tetrahydrofuran=1:1); diethyl ether was added to the residue to crystallize; the crystals were filtered off, washed with diethyl ether, and dried under aeration to yield the title compound (454 mg, 2.0 mmol, 82%) as pale brown 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-36d89d62931b4ca4895c46cc939c94b5 |
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| Source note | uspto-grants-2006_09 |
|---|