HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 536245Generated: October 30, 2026
Diisopropylethylamine → HCID 178493823, compound
https://huagongshe.com/reaction/536245
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | PyBOP | HCID 2724699 | — |
| Reactant | 2-aminopyrimidine-5-carboxylic Acid | HCID 7020367 | — |
| Reactant | HCID 178493824 | HCID 178493824 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 178493823 | HCID 178493823 | 12.1% |
Reaction Steps
7-Methoxy-8-{[4-(methylsulfonyl)benzyl]oxy}-2,3-dihydroimidazo[1,2-c]quinazolin-5-amine (Step 1, 76 mg, 0.19 mmol) was dissolved in DMF (5 mL), and 2-aminopyrimidine-5-carboxylic acid (40 mg, 0.29 mmol) was added. PyBOP (152 mg, 0.29 mmol) and diisopropylethylamine (0.15 mL, 0.85 mmol) were subsequently added. The mixture was stirred at it overnight, during which a tan solid precipitated. The DMF was removed under reduced pressure and the residue purified via silica gel chromatography (0-3% MeOH/CH2Cl2+0.1% Et3N). The solvent was evaporated under reduced pressure, the residue triturated in water (5 mL), collected by vacuum filtration, then washed with acetone. High vacuum drying gave the title compound (12 mg, 12%): HPLC MS RT=2.06 min, MH+=522.1; 1H NMR (DMSO-d6+2 drops TFA-d) δ: 3.22 (3H, s), 4.00 (3H, s), 4.19-4.25 (2H, m), 4.48-4.55 (2H, m), 5.53 (2H, s), 7.53 (1H, d), 7.77 (2H, d), 7.97-8.03 (3H, m), 9.06 (2H, s).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08859572B2 |
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| Source dataset | uspto-grants-2014_10 |
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| ORD ID | ord-4511cf258c8f412eb912933c7e37f00a |
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| Source note | uspto-grants-2014_10 |
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