Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2221480Generated: November 1, 2026

HCID 10387575, compound → HCID 10339368, compound

https://huagongshe.com/reaction/2221480

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 10387575HCID 10387575—
ReactantHCID 21892247HCID 21892247—
ProductHCID 10339368HCID 10339368—

Reaction Steps

1-(2,4-Difluorobenzyl)-3-dimethylaminomethyl-1H-pyrrolo[2,3-c]pyridine-5-carboxylic acid. The title compound was prepared by hydrolysis of ethyl 1-(2,4-difluorobenzyl)-3-dimethylaminomethyl-1H-pyrrolo[2,3]-ccarboxylate in a manner similar to step (b) of example 1. 1H NMR (DMSO-d6) δ: 8.91 (s, 1H), 8.43 (s, 1H), 7.74 (s, 1H), 7.29-7.37 (m, 2H), 7.04-7.10 (m, 1H), 5.62 (s, 2H), 3.70 (s, 2H), 2.22 (s, 6H). LCMS (API-ES, M+H+): 346.3. (b) 1-(2,4-Difluorobenzyl)-3-dimethylaminomethyl-N-hydroxy-N-methyl-1H-pyrrolo[2,3-c]pyridine-5-carboxamide. The title compound was prepared by coupling of 1-(2,4-difluorobenzyl)-3- dimethylaminomethyl-1H-pyrrol (DMSO-d6)δ: 9.44 (broad s, 1H), 8.96 (s, 1H), 8.26 (s, 1H), 7.93 (s, 1H), 7.44 (m, 1H), 7.28-7.35 (m, 1H), 7.10 (m, 1H), 5.66 (s, 2H), 4.47 (s, 2H), 3.32 (s, 3H), 2.72 (s, 6H). LCMS (APCI, M+H+): 375.0. HRMS calcd for C19H21F2N4O2. (M+H) 375.1633, found 375.1632. HPLC: 97.62% purity.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07368571B2
Source datasetuspto-grants-2008_05
ORD IDord-4df7d81468174290a754f078054a9697
Source noteuspto-grants-2008_05