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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1792962Generated: November 4, 2026

Carbamimidoylazanium Chloride → HCID 178422545, compound

https://huagongshe.com/reaction/1792962

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbamimidoylazanium ChlorideHCID 5460839—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantHCID 86591371HCID 86591371—
SolventWaterHCID 962—
ProductHCID 178422545HCID 17842254570.2%

Reaction Conditions

Temperature20 °C

Reaction Steps

N-[(2-Isobutyl-5-methyl-3-oxo-2,3-dihydro-1H-isoindol-1-yl)acetyl]guanidine is prepared as described in Example 1, starting with 1.75 g of potassium tert-butoxide, 1.78 g of guanidinium chloride and 0.9 g of ethyl (2-isobutyl-5-methyl-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 40 hours and is then poured into 150 cm3 of water and extracted with 3 times 150 cm3 of ethyl acetate. The organic extracts are combined, washed with-3 times 50 cm3 of water, dried over magnesium sulphate, filtered and then concentrated to dryness under reduced pressure (2.7 kPa) at a temperature in the region of 40° C. The residue is taken up in diethyl ether and then filtered, giving 0.66 g of N-[(2-isobutyl-5-methyl-3-oxo-2,3-dihydro-1H-isoindol-1-yl)acetyl]guanidine in the form of a white solid melting at 266° C. (Analysis C16H22N4O2% calculated C : 63.56, H : 7.33, N: 18.53, O: 10.58% found C : 63.57, H: 7.48, N: 18.50).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07078428B2
Source datasetuspto-grants-2006_07
ORD IDord-b94f6d23a63143b8aab50c54215d1082
Source noteuspto-grants-2006_07