HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 536215Generated: October 30, 2026
Trifluoroacetic acid → HCID 178493836, compound
https://huagongshe.com/reaction/536215
Participants
| Role | Name | HCID | Charge |
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| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | 7-methoxy-8-phenylmethoxy-2,3-dihydroimidazo[1,2-c]quinazolin-5-amine | HCID 178493820 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 178493836 | HCID 178493836 | 100% |
Reaction Steps
3-(Benzyloxy)-6-(4,5-dihydro-1H-imidazol-2-yl)-2-methoxyaniline (Step 7, 30 g, 93 mmol) was added portionwise over 1 h to a round bottom flask containing TFA (400 mL) precooled with an ice bath. The reaction mixture was heated to 60° C. and allowed to stir at this temperature for 17 h at which time it was cooled to rt and the reaction mixture concentrated under reduced pressure. The resulting residue was taken up in DCM and hexanes and concentrated under reduced pressure. The material thus obtained was dissolved in MeOH and DCM (250 mL, 1:1) and concentrated under reduced pressure. The resulting solid was dried overnight under vacuum with low heat to give the title compound (100%): 1H NMR (DMSO-d6) δ: 7.61 (1H, m), 6.87 (1H, m), 4.15 (2H, br t), 4.00 (2H, m), 3.64 (3H, 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-95b3caaf46d14070b18d160e80b9664e |
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| Source note | uspto-grants-2014_10 |
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