Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2060918Generated: October 31, 2026

3-(Cyclopropylaminocarbonyl)phenylboronic acid → HCID 16124310, compound

https://huagongshe.com/reaction/2060918

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(Cyclopropylaminocarbonyl)phenylboronic acidHCID 3874247—
ReactantHCID 16124309HCID 16124309—
ProductHCID 16124310HCID 16124310—

Reaction Steps

The title compound was synthesized from 5-chloro-N-(2-(dimethylamino)ethyl)-3,8-dimethyl-9H-pyrido[2,3-b]indole-7-carboxamide and 3-(cyclopropylcarbamoyl)phenyl boronic acid using an analogous procedure to that described in the preparation of Compound 84. 1H NMR (400 MHz, DMSO-d6) δ ppm 0.57 (dd, J=3.92, 2.40 Hz, 2H) 0.71 (dd, J=6.95, 2.40 Hz, 2H) 1.23 (s, 1H) 2.26 (s, 3H) 2.65 (s, 3H) 2.87 (d, J=5.05 Hz, 6H) 3.29 (q, J=5.98 Hz, 2H) 3.61 (q, J=6.15 Hz, 2H) 7.20 (s, 1H) 7.50 (s, 1H) 7.66 (t, J=7.83 Hz, 1H) 7.77 (d, J=7.83 Hz, 1H) 7.98 (d, J=7.83 Hz, 1H) 8.08 (s, 1H) 8.31 (d, J=1.77 Hz, 1H) 8.57-8.61 (m, 1H) 8.59 (d, J=4.55 Hz, 1H) 12.05 (s, 1H). [M+H] calc'd for C28H31N5O2 470; found, 470.4.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08278450B2
Source datasetuspto-grants-2012_10
ORD IDord-1eefcb619d2d49eb848d5ddf56acfc06
Source noteuspto-grants-2012_10