HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 733003Generated: October 30, 2026
Ethylenediamine → HCID 21874780, compound
https://huagongshe.com/reaction/733003
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethylenediamine | HCID 3301 | — |
| Reactant | HCID 21874566 | HCID 21874566 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 21874780 | HCID 21874780 | — |
Reaction Steps
A suspension of 7-(2-furyl)-3-(6-phthalimidomethyl-2-pyridylmethyl)-3H-[1,2,3]triazolo[4,5-d]pyrimidine-5-amine (210 mg, 0.465 mmol) in EtOH (50 mL) was treated with ethylenediamine (62 μl, 0.929 mmol), stirred for 3 h at 90° C. and the resulting clear solution, cooled to room temperature and concentrated in vacuo to give 3-(6-aminomethyl-2-pyridylmethyl)-7-(2-furyl)-3H-[1,2,3]triazolo[4,5-d]pyrimidine-5-amine. A solution of this material in pyridine (10 mL) at 0° C. was treated with acetyl chloride (109 ml, 1.53 mmol), stirred for 10 min, poured into water (70 mL), extracted with EtOAc (3×20 mL) and the combined organic phase was dried (MgSO4), concentrated in vacuo and purified by chromatography [SiO2; EtOAc] to give the title compound (110 mg, 65%) as a beige solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07589097B2 |
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| Source dataset | uspto-grants-2009_09 |
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| ORD ID | ord-899306cb00324c6080b33723229e3f8b |
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| Source note | uspto-grants-2009_09 |
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