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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1620191Generated: October 30, 2026

Thionyl Chloride → HCID 68182136, compound

https://huagongshe.com/reaction/1620191

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
ReactantHCID 68182334HCID 68182334—
SolventDichloromethaneHCID 6344—
ProductHCID 68182136HCID 6818213690%

Reaction Steps

To a solution of (2-(ethylamino)-6-methylquinolin-3-yl)methanol RBO 35160 (460 mg, 2.13 mmol) in CH2Cl2 (30 mL) in a round-bottomed flask equipped with a magnetic stirrer was added thionyl chloride (1.55 mL, 21.3 mmol). The mixture was stirred for 2 h at RT, evaporated under vacuum at 45° C., coevaporated twice with CH2Cl2 to remove SOCl2 to afford 3-(chloromethyl)-N-ethyl-6-methylquinolin-2-amine hydrochloride RBO 35162 as a yellow solid (520 mg, 90% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08772316B2
Source datasetuspto-grants-2014_07
ORD IDord-d4bb866372044a5c803e28f9dc639202
Source noteuspto-grants-2014_07