HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2400301Generated: October 30, 2026
Trifluoroacetic acid → HCID 70144271, compound
https://huagongshe.com/reaction/2400301
Participants
| Role | Name | HCID | Charge |
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| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | HCID 56968072 | HCID 56968072 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 70144271 | HCID 70144271 | — |
Reaction Steps
As shown in Scheme 2, a mixture of intermediate 1 of Scheme 2 (16 mg) and intermediate 3 of Scheme 1 (1-(3-(4-amino-3-methoxyphenylamino)azetidin-1-yl)ethanone, 20 mg) in dioxane (1.0 mL) with catalytic trifluoroacetic acid was stirred overnight at 50° C. The crude was concentrated under reduced pressure and purified using HPLC (TFA modifier) to give the title compound (12 mg) as a TFA salt. 1H-NMR (DMSO-d6, 400 MHz) δ 10.6 (s, 1H), 10.15 (s, 1H), 9.45 (s, 1H), 8.62 (br, 1H), 6.96-7.85 (m, 4H), 6.55 (dd, J=2, 10 Hz, 1H), 6.23 (d, J=10 Hz, 1H), 5.74 (d, J=10 Hz, 1H), 3.15-3.85 (m, 6H), 1.77 (s, 3H); calculated mass for C26H26F3N7O3: 541.2. found: 542.2 (M+H+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08796255B2 |
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| Source dataset | uspto-grants-2014_08 |
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| ORD ID | ord-af0a812d0e0b45dd988ffe0521cd9b4d |
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| Source note | uspto-grants-2014_08 |
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