3,4-dihydro-3-[4-methoxybenzyl(phenylacetyl)amino]-2-oxobenz[e][1,3]oxazine-7-carboxylic acid

Base Information

Chemical Name:3,4-dihydro-3-[4-methoxybenzyl(phenylacetyl)amino]-2-oxobenz[e][1,3]oxazine-7-carboxylic acid
CAS No.:330580-67-1
Molecular Formula:C₂₅H₂₂N₂O₆
Molecular Weight:446.459
Hs Code.:

Synonyms:3,4-dihydro-3-[4-methoxybenzyl(phenylacetyl)amino]-2-oxobenz[e][1,3]oxazine-7-carboxylic acid

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Chemical Property of 3,4-dihydro-3-[4-methoxybenzyl(phenylacetyl)amino]-2-oxobenz[e][1,3]oxazine-7-carboxylic acid

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Technology Process of 3,4-dihydro-3-[4-methoxybenzyl(phenylacetyl)amino]-2-oxobenz[e][1,3]oxazine-7-carboxylic acid

There total 8 articles about 3,4-dihydro-3-[4-methoxybenzyl(phenylacetyl)amino]-2-oxobenz[e][1,3]oxazine-7-carboxylic acid 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: 60.0%

: 530-62-1
1,1'-carbonyldiimidazole

: 330580-66-0
3-hydroxy-4-{[2-(4-methoxybenzyl)-2-(phenylacetyl)hydrazino]methyl}benzoic acid

: 330580-67-1
3,4-dihydro-3-[4-methoxybenzyl(phenylacetyl)amino]-2-oxobenz[e][1,3]oxazine-7-carboxylic acid

Guidance literature:: With triethylamine; In tetrahydrofuran; for 4h; Heating;
DOI:10.1002/1099-0690(200101)2001:1<141::aid-ejoc141>3.0.co;2-j

Reference yield:

: 619-12-5
4-formyl-3-hydroxybenzoic acid

: 330580-67-1
3,4-dihydro-3-[4-methoxybenzyl(phenylacetyl)amino]-2-oxobenz[e][1,3]oxazine-7-carboxylic acid

Guidance literature:: Multi-step reaction with 3 steps

1: 67 percent / Et₃N / methanol / 16 h / Heating

2: 68 percent / NaBH₃CN; CF₃CO₂H / methanol / 16 h / 20 °C / pH 3

3: 60 percent / Et₃N / tetrahydrofuran / 4 h / Heating

With sodium cyanoborohydride; triethylamine; trifluoroacetic acid; In tetrahydrofuran; methanol;
DOI:10.1002/1099-0690(200101)2001:1<141::aid-ejoc141>3.0.co;2-j

Reference yield:

: 2393-23-9
4-methoxy-benzylamine

: 330580-67-1
3,4-dihydro-3-[4-methoxybenzyl(phenylacetyl)amino]-2-oxobenz[e][1,3]oxazine-7-carboxylic acid

Guidance literature:: Multi-step reaction with 6 steps

1: 73 percent / 1 N NaOH / 3 h / 20 °C

2: AcOH; Ac₂O; NaNO₂ / 0 - 20 °C

3: 0.48 g / Zn dust; AcOH / ethyl acetate / 3 h / 20 °C

4: 67 percent / Et₃N / methanol / 16 h / Heating

5: 68 percent / NaBH₃CN; CF₃CO₂H / methanol / 16 h / 20 °C / pH 3

6: 60 percent / Et₃N / tetrahydrofuran / 4 h / Heating

With sodium hydroxide; acetic anhydride; sodium cyanoborohydride; acetic acid; triethylamine; trifluoroacetic acid; zinc; sodium nitrite; In tetrahydrofuran; methanol; ethyl acetate;
DOI:10.1002/1099-0690(200101)2001:1<141::aid-ejoc141>3.0.co;2-j