HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1787557Generated: October 30, 2026
Diisopropylethylamine → HCID 178474220, compound
https://huagongshe.com/reaction/1787557
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 6-(Acetylamino)nicotinic acid | HCID 419744 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 178419695 | HCID 178419695 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 178474220 | HCID 178474220 | 31.6% |
Reaction Steps
To a mixture of 8-(morpholin-4-yl)-2,3-dihydroimidazo[1,2-c]quinazolin-5-amine hydrobromide 105.7 mg (0.30 mmol), 6-(acetamido)nicotinic acid 81.1 mg (0.45 mmol) and N,N-diisopropylethylamine 0.26 mL (1.50 mmol) in N,N-dimethylformamide 2 mL was added PyBOP((1H-1,2,3-benzotriazol-1-yloxy)(tripyrrolidin-1-yl)-phosphonium hexafluorophosphate) 234.2 mg (0.45 mmol) and stirred at 90° C. for 16 hours. After cooling to room temperature, saturated NaHCO3 solution was added. The precipitate was collected and washed with water, methanol, and diethyl ether to give the title compound 41.1 mg as yellow solid. Yield 31.6%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07511041B2 |
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| Source dataset | uspto-grants-2009_03 |
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| ORD ID | ord-4cb9f5ffb60e4973b48f0fd65fd117a7 |
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| Source note | uspto-grants-2009_03 |
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