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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2422931Generated: November 1, 2026

Aniline → HCID 86628706, compound

https://huagongshe.com/reaction/2422931

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAnilineHCID 6115—
ReactantDimethylformamideHCID 6228—
ReactantDiisopropylethylamineHCID 81531—
Reactant4-(tert-butoxycarbonylamino)-3-(4-chlorophenyl)butanoic acidHCID 13100840—
ProductHCID 86628706HCID 8662870656,021.898%

Reaction Steps

To a solution of 33 (0.206 g, 0.657 mmol, 1.2 eq) and aniline (0.051 g, 0.548 mmol) in dry DMF (5 ml) HATU (0.315 g, 0.9087 mmol, 1.5 eq) and DIPEA (0.340 g, 2.63 mmol, 4 eq) was added at room temperature under Ar. After stirring overnight at room temperature, the reaction mixture was quenched with water (10 mL) and extracted with ethyl acetate (2×15 ml). The organic extracts were collected, dried over Na2SO4 and the solvent was distilled off under reduced pressure. The crude compound was purified by chromatography on silica gel (3:7 ethyl acetate/hexane, v/v, Rf 0.30) to give 34 as a white solid (0.120 g, 0.307 mol, 47%), mp 165-167° C. 1H NMR (400 MHz, CDCl3) δ 1.43 (9H, s), 2.55 (1H, dd, J 5.0, 13.8 Hz), 2.75 (1H, dd, J 8.4, 13.6 Hz), 3.16-3.39 (2H, m), 3.52-3.57 (1H, m), 4.60 (1H, bs), 7.07-7.13 (3H, m), 7.29-7.32 (4H, m), 7.54 (2H, d, J 8.4 Hz), 8.61 (1H, bs).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07960434B2
Source datasetuspto-grants-2011_06
ORD IDord-6ac6adeef90945bbac55809ee3f82f8d
Source noteuspto-grants-2011_06