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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2060923Generated: October 31, 2026

3-(Cyclopropylaminocarbonyl)phenylboronic acid → HCID 25017261, compound

https://huagongshe.com/reaction/2060923

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(Cyclopropylaminocarbonyl)phenylboronic acidHCID 3874247—
Reactant5-Chloro-3,8-dimethyl-N-(1-methyl-4-piperidinyl)-9H-pyrido[2,3-b]indole-7-carboxamideHCID 16124308—
ProductHCID 25017261HCID 25017261—

Reaction Steps

The title compound was synthesized from 5-chloro-3,8-dimethyl-N-(1-methylpiperidin-4-yl)-9H-pyrido[2,3-b]indole-7-carboxamide and 3-(cyclopropylcarbamoyl)phenylboronic acid using an analogous procedure to that described in the preparation of compound 88. 1H NMR (400 MHz, DMSO-d6) δ ppm 0.80 (d, J=5.81 Hz, 4H) 1.53 (qd, J=11.62, 3.03 Hz, 2H) 1.82 (br. s., 1H) 1.79 (d, J=5.56 Hz, 2 H) 1.95 (t, J=10.86 Hz, 2H) 2.15 (s, 3H) 2.27 (s, 3H) 2.59 (s, 3H) 2.74 (br. d, J=10.86 Hz, 2H) 3.75 (dt, J=7.33, 3.66 Hz, 1H) 6.98 (s, 1H) 7.27 (d, J=7.58 Hz, 1H) 7.49 (t, J=7.83 Hz, 1H) 7.69 (br. s., 2H) 7.91 (s, 1H) 8.24-8.31 (m, 2H) 10.37 (s, 1H) 11.92 (br. s., 1H) [M+H] calc'd for C30H34N5O2, 496.3; found, 496.4.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08278450B2
Source datasetuspto-grants-2012_10
ORD IDord-c923d23364be4ff89507e260a8176327
Source noteuspto-grants-2012_10