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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1433886Generated: November 3, 2026

Isonicotinoyl chloride hydrochloride → Ethyl[5-methoxy-2-(6-methoxy-1,2,3,4-tetrahydronaphthalen-2-yl)phenyl]pyridin-4-ylmethylamine

https://huagongshe.com/reaction/1433886

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsonicotinoyl chloride hydrochlorideHCID 12262826—
ReactantEthyl[5-methoxy-2-(6-methoxy-1,2,3,4-tetrahydronaphthalen-2-yl)phenyl]amineHCID 23087318—
ReactantPyridine-4-carboxylic acid ethyl [5-methoxy-2-(6-methoxy-1,2,3,4-tetrahydronaphthalen-2-yl)phenyl]amideHCID 66626131—
ProductEthyl[5-methoxy-2-(6-methoxy-1,2,3,4-tetrahydronaphthalen-2-yl)phenyl]pyridin-4-ylmethylamineHCID 6662571127.3%

Reaction Steps

Synthesized from ethyl[5-methoxy-2-(6-methoxy-1,2,3,4-tetrahydronaphthalen-2-yl)phenyl]amine and isonicotinoyl chloride hydrochloride according to an analogous synthetic method to Preparation Example 86, pyridine-4-carboxylic acid ethyl [5-methoxy-2-(6-methoxy-1,2,3,4-tetrahydronaphthalen-2-yl)phenyl]amide (163 mg) was used according to an analogous synthetic method to Example 337 described below to provide ethyl[5-methoxy-2-(6-methoxy-1,2,3,4-tetrahydronaphthalen-2-yl)phenyl]pyridin-4-ylmethylamine (43 mg). The total amount of this compound was used according to an analogous synthetic method to Example 111 described below to provide the title compound (42 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07612114B2
Source datasetuspto-grants-2009_11
ORD IDord-7ff433d39e734c38ab0abc3229b4fb01
Source noteuspto-grants-2009_11