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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1093670Generated: October 31, 2026

1-Hydroxybenzotriazole → HCID 57874516, compound

https://huagongshe.com/reaction/1093670

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantDiisopropylethylamineHCID 81531—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
ReactantN-biphenyl-4-yl-malonamic acidHCID 55049154—
ReactantHCID 66591387HCID 66591387—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 57874516HCID 5787451651%

Reaction Steps

To a stirred solution of N-biphenyl-4-yl-malonamic acid (0.15 g, 0.00059 mole) in DMF (4 mL) was added DIPEA (0.226 g, 0.00176 mole), HOBt (0.095 g, 0.00071 mole) and EDCI.HCl (0.134 g, 0.00071 mole). After 2 minutes 4-(2-bromo-phenylsulfanyl)-piperidine hydrochloride (0.21 g, 0.00071 mole) was added and the resulting mixture was stirred overnight. The reaction mixture was then diluted with cold water and the resulting precipitate was isolated by filtration. Purification by column chromatography using silica gel 60-120 mesh (60% ethyl acetate in hexane) afforded 0.153 g (51%) of N-biphenyl-4-yl-3-[4-(2-bromo-phenylsulfanyl)-piperidin-1-yl]-3-oxo-propionamide. LC-MS purity: 509.08 (M+1)+, 87.3%, 1H NMR (DMSO-d6): δ 10.2 (s, 1H), 7.82-7.6 (m, 6H), 7.48-7.36 (m, 3H), 7.36-7.28 (m, 1H), 7.22-7.12 (m, 1H), 5.6-5.2 (d, 1H), 4.25 (d, 1H), 3.7 (m, 1H), 3.55 (s, 2H), 2.95 (m, 1H), 2.0 (m, 2H), 1.7-1.5 (m, 1H), 1.5-1.35 (m, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08129376B2
Source datasetuspto-grants-2012_03
ORD IDord-151523ccbe944db49b674cf4ca1b0c75
Source noteuspto-grants-2012_03