HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 733219Generated: October 31, 2026
Carbamimidoylazanium Chloride → HCID 178513088, compound
https://huagongshe.com/reaction/733219
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Carbamimidoylazanium Chloride | HCID 5460839 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Reactant | HCID 69714143 | HCID 69714143 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 178513088 | HCID 178513088 | 76.4% |
Reaction Steps
N-[(2-Cyclopropylmethyl-3-oxo-2,3-dihydro-1H-isoindol-1-yl)acetyl]guanidine is prepared as described in Example 1, starting with 2.9 g of potassium tert-butoxide, 2.5 g of guanidinium chloride and 1.5 g of ethyl (2-cyclopropylmethyl-3-oxo-2,3-dihydro-1H-isoindol-1-yl)acetate. The reaction mixture is stirred at a temperature in the region of 20° C. for 20 hours, followed by addition of 20 cm3 of water. The aqueous phase is extracted with 3 times 100 cm3 of ethyl acetate. The organic extracts are combined and then concentrated to dryness under reduced pressure (0.6 kPa) at a temperature in the region of 35° C. The residue is taken up in water, triturated, filtered off and then dried in a desiccator. 1.2 g of N-[(2-cyclopropylmethyl-3-oxo-2,3-dihydro-1H-isoindol-1-yl)acetyl]guanidine are thus obtained in the form of an off-white powder melting at 229° C. Mass spectrum: DCI: m/e 287 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07589117B2 |
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| Source dataset | uspto-grants-2009_09 |
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| ORD ID | ord-f34c07540850460b861dc019f4761fe0 |
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| Source note | uspto-grants-2009_09 |
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