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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1432019Generated: November 1, 2026

Acetic Acid → (R)-3-((1-((R)-6-((2,2-dimethylethylamino)methyl)-1,2,3,4-tetrahydronaphthalen-1-yl)-1H-1,2,3-triazol-4-yl)methyl)-4-(4-methylbenzenesulfonyl)-3,4-dihydropyrazin-2(1H)-one

https://huagongshe.com/reaction/1432019

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantTert-ButylamineHCID 6385—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant(R)-5-(4-(((R)-3-Oxo-1-(4-methylbenzenesulfonyl)-1,2,3,4-tetrahydropyrazin-2-yl)-methyl)-1H-1,2,3-triazol-1-yl)-5,6,7,8-tetrahydronaphthalene-2-carbaldehydeHCID 57932484—
Solvent1,2-DichloroethaneHCID 11—
Product(R)-3-((1-((R)-6-((2,2-dimethylethylamino)methyl)-1,2,3,4-tetrahydronaphthalen-1-yl)-1H-1,2,3-triazol-4-yl)methyl)-4-(4-methylbenzenesulfonyl)-3,4-dihydropyrazin-2(1H)-oneHCID 11570253—

Reaction Steps

(R)-5-(4-(((R)-3—Oxo-1-(4-methylbenzenesulfonyl)-1,2,3,4-tetrahydropyrazin-2-yl)-methyl)-1H-1,2,3-triazol-1-yl)-5,6,7,8-tetrahydronaphthalene-2-carbaldehyde (1.1 mmol, 1 eq) was dissolved in DCE and treated with 4 Å powdered molecular sieves. To the solution was added t-butyl amine (3.2 mmol, 3.0 eq) and AcOH (3.2 mmol, 3.0 eq). The reaction stirred at RT overnight. NaBH(OAc)3 (3.3 mmol, 3.0 eq) was added and after 3 h, the solvent was removed and the residue was purified by SiO2 to afford amine the title compound (MS (m/z): 549.3 (m+H)).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07612060B2
Source datasetuspto-grants-2009_11
ORD IDord-01ef3e5eb36846e6a86e9dd102b51b25
Source noteuspto-grants-2009_11