HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1362962Generated: October 30, 2026
3-(Trifluoromethyl)benzylamine → HCID 11548849, compound
https://huagongshe.com/reaction/1362962
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3-(Trifluoromethyl)benzylamine | HCID 75962 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 58964276 | HCID 58964276 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | HCID 11548849 | HCID 11548849 | 65% |
Reaction Steps
4-[2-(7-Aza-bicyclo[2.2.1]hept-7-yl)-ethoxy]-3-(4-bromo-2-methyl-2H-pyrazol-3-yl)-phenylamine (50.0 mg, 0.13 mmol) was added to a solution of 4-nitrophenylchloroformate (26.0 mg, 0.13 mmol) in 1,2-dichloroethane (4.0 mL) and the mixture stirred at room temperature for 1 hour. To the resulting precipitate mixture was added 3-trifluoromethylbenzylamine (0.022 mL, 0.15 mmol) and N,N-diisopropylethylamine (0.030 mL, 0.17 mmol), and the mixture stirred an additional 1 hour. The mixture was concentrated and purified by RP-HPLC. The collected fractions were concentrated and 12% sodium hydroxide (aq) (0.2 mL) was added to give pH 9. The solution was extracted into ethyl acetate and the organic layer was dried over sodium sulfate, filtered, and evaporated to dryness to give a white solid (49 mg, 65%). LCMS m/z (%)=592 (M+H 79Br, 100), 594 (M+H 81Br, 67). 1H NMR (400 MHz, DMSO-d6) δ: 8.67 (bs, 1H), 7.67 (bs, 1H), 7.65-7.59 (m, 4H), 7.53-7.50 (m, 1H), 7.33 (d, J=2.69 Hz, 1H), 7.12 (d, J=9.04 Hz, 1H), 6.77-6.74 (m, 1H), 4.40 (d, J=4.0 Hz, 2H), 4.08-3.98 (m, 2H), 3.67 (s, 3H), 3.12 (m, 2H), 2.59-2.55 (m, 2H), 1.56-1.54 (m, 4H), 1.17-1.15 (m, 4H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07884101B2 |
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| Source dataset | uspto-grants-2011_02 |
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| ORD ID | ord-e37ccf1bea534611ac2cf45bce253385 |
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| Source note | uspto-grants-2011_02 |
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