HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2389751Generated: October 29, 2026
Diisopropylethylamine → HCID 59312986, compound
https://huagongshe.com/reaction/2389751
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | tert-Butyl (2-aminopropyl)carbamate | HCID 22499135 | — |
| Reactant | HCID 59312932 | HCID 59312932 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 59312986 | HCID 59312986 | — |
Reaction Steps
5-Chloro-7-(2,4-dichlorophenyl)imidazo[1,2-c]pyrimidine (Example 6A) (800 mg, 2.7 mmol), tert-butyl (2-aminopropyl)carbamate (700 mg, 4.0 mmol) and N,N-diisopropylethylamine (1.00 g, 8.0 mmol) are dissolved in DMSO (13 ml) and stirred at 120° C. under argon for 12 hours. The reaction mixture is diluted with water (100 ml) and extracted with ethyl acetate (3×75 ml). The combined organic phases are washed with saturated aqueous sodium chloride solution, dried over magnesium sulphate and concentrated. Removal of the solvent results in a foam which is taken up in diethyl ether. The product precipitates as solid from the diethyl ether solution and is filtered off with suction and dried. 800 mg (68% of theory) of the product are obtained as a solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08273752B2 |
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| Source dataset | uspto-grants-2012_09 |
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| ORD ID | ord-cf53dc6daf8e417c94cf996c971758d8 |
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| Source note | uspto-grants-2012_09 |
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