HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1825422Generated: October 26, 2026
Diethyl Ether → 4-(2-{[2-(2-Pyridylamino)ethyl]amino}pyrimidin-4-yl)benzamide
https://huagongshe.com/reaction/1825422
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Ethylenediamine | HCID 3301 | — |
| Reactant | 2-Chloropyridine | HCID 7977 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | N~1~-(Pyridin-2-yl)ethane-1,2-diamine | HCID 410428 | — |
| Reactant | HCID 178512433 | HCID 178512433 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 4-(2-{[2-(2-Pyridylamino)ethyl]amino}pyrimidin-4-yl)benzamide | HCID 22142834 | — |
Reaction Steps
2-(2-Aminoethylamino)pyridine (prepared from 2-chloropyridine and ethylenediamine in accordance with the method described in T. Mega et al., 1988, Bull. Chem. Soc. Japan 61:4315, which is incorporated herein by reference) (6 mmol) was treated with benzotriazole carboxamidinium 4-methylbenzenesulfonatesulfonate (2.0 g, 6 mmol) and DIEA (1.05 ml, 6 mmol) in anhydrous acetonitrile (10 ml) for 65 hours. Ether (ca. 10 ml) was then added to this mixture. After 8 hours the white solid amino[2-(2-pyridylamino)ethyl]carboxamidinium 4-methylbenzenesulfonate was filtered off and dried in vacuo. The resulting guanidine (200 mg) was reacted with 100 mg of resin (21 hours, 90° C.) according to the method described in Example 10 (Resin method C), to give the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07045519B2 |
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| Source dataset | uspto-grants-2006_05 |
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| ORD ID | ord-32e787e57e8e431db9912c499a45cc02 |
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| Source note | uspto-grants-2006_05 |
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