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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1640173Generated: October 30, 2026

Ammonium Chloride → HCID 23584982, compound

https://huagongshe.com/reaction/1640173

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantSodium MethoxideHCID 10942334—
ReactantHCID 58902223HCID 58902223—
SolventMethanolHCID 887—
ProductHCID 23584982HCID 23584982—

Reaction Steps

To a solution of N-(3-tert-butylphenyl)-7-[(2-cyanopyridin-4-yl)oxy]-1,2,3,4-tetrahydronaphthalene-2-carboxamide (1.5 g, 3.5 mmol) in MeOH (20 mL) was added sodium methoxide (28 mg, 0.52 mmol). The solution was allowed to stir at rt for 3 days and then ammonium chloride (0.28 g, 5.3 mmol) was added. The reaction mixture was allowed to stir overnight and then concentrated to give 7-({2-[amino(imino)methyl]pyridin-4-yl}oxy)-N-(3-tert-butylphenyl)-1,2,3,4-tetrahydronaphthalene-2-carboxamide I-422 as a white solid, which was directly used into the next step. LCMS: (FA) ES+ 443.3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08110687B2
Source datasetuspto-grants-2012_02
ORD IDord-17a91f672d60404393bf726065d3503c
Source noteuspto-grants-2012_02