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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 423488Generated: October 29, 2026

{4-[(2-Methylpropyl)carbamoyl]phenyl}boronic acid → HCID 59177806, compound

https://huagongshe.com/reaction/423488

Reaction equation

Participants

RoleNameHCIDCharge
Reactant{4-[(2-Methylpropyl)carbamoyl]phenyl}boronic acidHCID 2773470—
Reactant4-(4-Bromophenoxymethyl)piperidine-1-carboxylic acid isopropyl esterHCID 57930300—
ProductHCID 59177806HCID 5917780623.2%

Reaction Steps

The title compound (21 mg, 19%) was prepared from (4-{[(2-methylpropyl)amino]carbonyl}phenyl)boronic acid (44 mg, 0.2 mmol) and 1-methylethyl 4-{[(4-bromophenyl)oxy]methyl}-1-piperidinecarboxylate (prepared as in Example 9, Step 2, 71 mg, 0.2 mmol) in a manner similar to Example 21, Step 3 and worked up in a manner similar to Example 9, Step 3. 1H NMR (400 MHz, CDCl3): δ 7.80 (d, 2H, J=8.6 Hz), 7.60 (d, 2H, J=8.6 Hz), 7.54 (d, 2H, J=8.8 Hz), 6.96 (d, 2H, J=8.9 Hz), 6.17 (t, 1H, J=5.8 Hz), 4.97-4.84 (m, 1H), 4.21 (bs, 2H), 3.85 (d, 2H, J=6.4 Hz), 3.34-3.27 (m, 2H), 2.83-2.73 (m, 2H), 2.05-1.95 (m, 1H), 1.95-1.89 (m, 1H), 1.90-1.80 (m, 2H), 1.35-1.26 (m, 2H), 1.24 (d, 6H, J=6.2 Hz), 0.99 (d, 6H, J=6.7 Hz); LRMS (ESI), m/z 453 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08101634B2
Source datasetuspto-grants-2012_01
ORD IDord-15f439eedb8a4aa5a86256fadc3fc781
Source noteuspto-grants-2012_01