tert-butyl 6-(5-(3-cyano-4-isopropoxyphenyl)-1,2,4-oxadiazol-3-yl)-3,4-dihydroisoquinoline-2(1H)-carboxylate

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Chemical Name:tert-butyl 6-(5-(3-cyano-4-isopropoxyphenyl)-1,2,4-oxadiazol-3-yl)-3,4-dihydroisoquinoline-2(1H)-carboxylate
CAS No.:1286751-23-2
Molecular Formula:C₂₆H₂₈N₄O₄
Molecular Weight:460.533
Hs Code.:

Synonyms:tert-butyl 6-(5-(3-cyano-4-isopropoxyphenyl)-1,2,4-oxadiazol-3-yl)-3,4-dihydroisoquinoline-2(1H)-carboxylate

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Chemical Property of tert-butyl 6-(5-(3-cyano-4-isopropoxyphenyl)-1,2,4-oxadiazol-3-yl)-3,4-dihydroisoquinoline-2(1H)-carboxylate

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Technology Process of tert-butyl 6-(5-(3-cyano-4-isopropoxyphenyl)-1,2,4-oxadiazol-3-yl)-3,4-dihydroisoquinoline-2(1H)-carboxylate

There total 5 articles about tert-butyl 6-(5-(3-cyano-4-isopropoxyphenyl)-1,2,4-oxadiazol-3-yl)-3,4-dihydroisoquinoline-2(1H)-carboxylate which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 69.5%

: 1072948-37-8
3-cyano-4-[(1-methylethyl)oxy]benzoyl chloride

: 1258856-46-0
6-(N-hydroxycarbamimidoyl)-3,4-dihydro-1H-isoquinoline-2-carboxylic acid t-butyl ester

: 1286751-23-2
tert-butyl 6-(5-(3-cyano-4-isopropoxyphenyl)-1,2,4-oxadiazol-3-yl)-3,4-dihydroisoquinoline-2(1H)-carboxylate

Guidance literature:: With pyridine; In toluene; at 20 - 120 ℃; for 2.33333h; Inert atmosphere;
DOI:10.1021/ml2000214

Reference yield:

: 258273-31-3
3-cyano-4-isopropoxybenzoic acid

: 1286751-23-2
tert-butyl 6-(5-(3-cyano-4-isopropoxyphenyl)-1,2,4-oxadiazol-3-yl)-3,4-dihydroisoquinoline-2(1H)-carboxylate

Guidance literature:: Multi-step reaction with 2 steps

1: oxalyl dichloride; N,N-dimethyl-formamide / dichloromethane / 4 h / 20 °C

2: pyridine / toluene / 2.33 h / 20 - 120 °C / Inert atmosphere

With pyridine; oxalyl dichloride; N,N-dimethyl-formamide; In dichloromethane; toluene;
DOI:10.1021/ml2000214

Reference yield:

: 166398-33-0
tert-butyl 6-cyano-3,4-dihydroisoquinoline-2(1H)-carboxylate

: 1286751-23-2
tert-butyl 6-(5-(3-cyano-4-isopropoxyphenyl)-1,2,4-oxadiazol-3-yl)-3,4-dihydroisoquinoline-2(1H)-carboxylate

Guidance literature:: Multi-step reaction with 2 steps

1: hydroxylamine hydrochloride; sodium hydrogencarbonate / ethanol / 4 h / 80 °C

2: pyridine / toluene / 2.33 h / 20 - 120 °C / Inert atmosphere

With pyridine; hydroxylamine hydrochloride; sodium hydrogencarbonate; In ethanol; toluene;
DOI:10.1021/ml2000214