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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1685477Generated: October 29, 2026

O-Phenylenediamine → tert-butyl (2R,4R)-2-((2-aminophenyl)carbamoyl)-4-(3-(4-cyanophenyl)ureido)piperidine-1-carboxylate

https://huagongshe.com/reaction/1685477

Reaction equation

Participants

RoleNameHCIDCharge
ReactantO-PhenylenediamineHCID 7243—
ReactantDiisopropylethylamineHCID 81531—
ReactantBenzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphateHCID 151348—
Reactant(2R,4R)-1-(tert-butoxycarbonyl)-4-(3-(4-cyanophenyl)ureido)piperidine-2-carboxylic AcidHCID 57539001—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Producttert-butyl (2R,4R)-2-((2-aminophenyl)carbamoyl)-4-(3-(4-cyanophenyl)ureido)piperidine-1-carboxylateHCID 5753906698.9%

Reaction Steps

Benzene-1,2-diamine (365 mg, 3.38 mmol) was added to a mixture of (2R,4R)-1-(tert-butoxycarbonyl)-4-(3-(4-cyanophenyl)ureido)piperidine-2-carboxylic acid (1400 mg, 3.60 mmol), BOP (1600 mg, 3.6 mmol) and DIEA (1.2 mL, 6.9 mmol) in DMF (20 mL), and the resulting solution was stirred at room temperature for 8 hours. Water (100 mL) was added to the reaction mixture and it was then extracted with ethyl acetate (2×200 mL). The organic layers were dried over MgSO4 and concentrated to give a red solid. Further purification by Companion (ReadySep, 80 g, silica gel packed) using ethyl acetate/heptane from 50-80% as eluent provided the title compound as a white solid 1600 mg (93%). LC-MS: 479.1, 477.2 (t=2.3 min).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08148401B2
Source datasetuspto-grants-2012_04
ORD IDord-c3123e3873aa40c380e3a26b607522e4
Source noteuspto-grants-2012_04