Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2227162Generated: October 30, 2026

4-Chlorobenzylamine → HCID 178432387, compound

https://huagongshe.com/reaction/2227162

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-ChlorobenzylamineHCID 66036—
ReactantHCID 178469685HCID 178469685—
SolventEthyl AcetateHCID 8857—
ProductHCID 178432387HCID 178432387—

Reaction Steps

A solution of ethyl 6-bromo-4-hydroxy-7-methyl[1,8]naphthyridine-3-carboxylate (Prep 1 0.57 g) and 4-chlorobenzylamine (2.59 g) is heated to 180° C. for 1 h. The mixture is cooled and diluted with EtOAc. The resulting precipitate is collected and dried. Physical characteristics are as follows: m.p. 269-270° C.; 1H NMR (DMSO-d6) δ 13.21, 10.09, 8.67, 8.62, 7.38, 4.54, 2.71; IR (drift) 3028, 2974, 2907, 1653, 1598, 1555, 1526, 1493, 1410, 1354, 1326, 1242, 1096, 806, 639 cm−1; Anal. Calcd for C17H13BrClN3O2: C, 50.21; H, 3.22; N, 10.33; Found: C, 50.31; H, 3.23; N, 10.17.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06413958B2
Source datasetuspto-grants-2002_07
ORD IDord-8b640b2181cb4ae3a104316a4d7a6675
Source noteuspto-grants-2002_07