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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1362962Generated: October 30, 2026

3-(Trifluoromethyl)benzylamine → HCID 11548849, compound

https://huagongshe.com/reaction/1362962

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(Trifluoromethyl)benzylamineHCID 75962—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 58964276HCID 58964276—
Solvent1,2-DichloroethaneHCID 11—
ProductHCID 11548849HCID 1154884965%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07884101B2
Source datasetuspto-grants-2011_02
ORD IDord-e37ccf1bea534611ac2cf45bce253385
Source noteuspto-grants-2011_02