methyl 2-cyano-5-diallyloxyphosphinyl-6-methyl-4-(3-nitrophenyl)-1,4-dihydropyridine-3-carboxylate

Base Information

Chemical Name:methyl 2-cyano-5-diallyloxyphosphinyl-6-methyl-4-(3-nitrophenyl)-1,4-dihydropyridine-3-carboxylate
CAS No.:115550-34-0
Molecular Formula:C₂₁H₂₂N₃O₇P
Molecular Weight:459.395
Hs Code.:

Synonyms:methyl 2-cyano-5-diallyloxyphosphinyl-6-methyl-4-(3-nitrophenyl)-1,4-dihydropyridine-3-carboxylate

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Chemical Property of methyl 2-cyano-5-diallyloxyphosphinyl-6-methyl-4-(3-nitrophenyl)-1,4-dihydropyridine-3-carboxylate

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Technology Process of methyl 2-cyano-5-diallyloxyphosphinyl-6-methyl-4-(3-nitrophenyl)-1,4-dihydropyridine-3-carboxylate

There total 5 articles about methyl 2-cyano-5-diallyloxyphosphinyl-6-methyl-4-(3-nitrophenyl)-1,4-dihydropyridine-3-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: 93.0%

: 117966-29-7
5-(Bis-allyloxy-phosphoryl)-2-(hydroxyimino-methyl)-6-methyl-4-(3-nitro-phenyl)-1,4-dihydro-pyridine-3-carboxylic acid methyl ester

: 115550-34-0
methyl 2-cyano-5-diallyloxyphosphinyl-6-methyl-4-(3-nitrophenyl)-1,4-dihydropyridine-3-carboxylate

Guidance literature:: With 1,1'-carbonyldiimidazole; In dichloromethane; for 48h; Heating;
DOI:10.1248/cpb.35.4819

Reference yield:

: 60705-25-1
4,4-dimethoxy-3-oxo-butyric acid methyl ester

: 115550-34-0
methyl 2-cyano-5-diallyloxyphosphinyl-6-methyl-4-(3-nitrophenyl)-1,4-dihydropyridine-3-carboxylate

Guidance literature:: Multi-step reaction with 5 steps

1: 85 percent / NH₃ / methanol / 20 h

2: 63 percent / acetonitrile / 36 h / Heating

3: 53 percent / 6 N HCl / acetone / 96 h / 0 - 10 °C

4: hydroxylamine hydrochloride, NaOAc / methanol; H₂O / 2 h / Ambient temperature

5: 93 percent / CDI / CH₂Cl₂ / 48 h / Heating

With hydrogenchloride; hydroxylamine hydrochloride; ammonia; sodium acetate; 1,1'-carbonyldiimidazole; In methanol; dichloromethane; water; acetone; acetonitrile;
DOI:10.1248/cpb.35.4819

Reference yield:

: 85396-57-2
methyl 3-amino-4,4-dimethoxy-2-butanoate

: 115550-34-0
methyl 2-cyano-5-diallyloxyphosphinyl-6-methyl-4-(3-nitrophenyl)-1,4-dihydropyridine-3-carboxylate

Guidance literature:: Multi-step reaction with 4 steps

1: 63 percent / acetonitrile / 36 h / Heating

2: 53 percent / 6 N HCl / acetone / 96 h / 0 - 10 °C

3: hydroxylamine hydrochloride, NaOAc / methanol; H₂O / 2 h / Ambient temperature

4: 93 percent / CDI / CH₂Cl₂ / 48 h / Heating

With hydrogenchloride; hydroxylamine hydrochloride; sodium acetate; 1,1'-carbonyldiimidazole; In methanol; dichloromethane; water; acetone; acetonitrile;
DOI:10.1248/cpb.35.4819