4-{4-[3-(3-carbamimidoyl-phenyl)-isoxazol-5-ylmethyl]-3-oxo-3,4-dihydro-2H-benzo[1,4]oxazin-7-yloxy}-piperidine-1-carboxylic acid tert-butyl ester

Base Information

Chemical Name:4-{4-[3-(3-carbamimidoyl-phenyl)-isoxazol-5-ylmethyl]-3-oxo-3,4-dihydro-2H-benzo[1,4]oxazin-7-yloxy}-piperidine-1-carboxylic acid tert-butyl ester
CAS No.:544694-98-6
Molecular Formula:C₂₉H₃₃N₅O₆
Molecular Weight:547.611
Hs Code.:

4-{4-[3-(3-carbamimidoyl-phenyl)-isoxazol-5-ylmethyl]-3-oxo-3,4-dihydro-2<i>H</i>-benzo[1,4]oxazin-7-yloxy}-piperidine-1-carboxylic acid <i>tert</i>-butyl ester

Synonyms:4-{4-[3-(3-carbamimidoyl-phenyl)-isoxazol-5-ylmethyl]-3-oxo-3,4-dihydro-2H-benzo[1,4]oxazin-7-yloxy}-piperidine-1-carboxylic acid tert-butyl ester

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Chemical Property of 4-{4-[3-(3-carbamimidoyl-phenyl)-isoxazol-5-ylmethyl]-3-oxo-3,4-dihydro-2H-benzo[1,4]oxazin-7-yloxy}-piperidine-1-carboxylic acid tert-butyl ester

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Technology Process of 4-{4-[3-(3-carbamimidoyl-phenyl)-isoxazol-5-ylmethyl]-3-oxo-3,4-dihydro-2H-benzo[1,4]oxazin-7-yloxy}-piperidine-1-carboxylic acid tert-butyl ester

There total 10 articles about 4-{4-[3-(3-carbamimidoyl-phenyl)-isoxazol-5-ylmethyl]-3-oxo-3,4-dihydro-2H-benzo[1,4]oxazin-7-yloxy}-piperidine-1-carboxylic acid tert-butyl ester 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:

: 4-(4-{3-[3-(N-hydroxycarbamimidoyl)-phenyl]-isoxazol-5-ylmethyl}-3-oxo-3,4-dihydro-2H-benzo[1,4]oxazin-7-yloxy)-piperidine-1-carboxylic acid tert-butyl ester

: 544694-98-6
4-{4-[3-(3-carbamimidoyl-phenyl)-isoxazol-5-ylmethyl]-3-oxo-3,4-dihydro-2H-benzo[1,4]oxazin-7-yloxy}-piperidine-1-carboxylic acid tert-butyl ester

Guidance literature:: 4-(4-{3-[3-(N-hydroxycarbamimidoyl)-phenyl]-isoxazol-5-ylmethyl}-3-oxo-3,4-dihydro-2H-benzo[1,4]oxazin-7-yloxy)-piperidine-1-carboxylic acid tert-butyl ester; With acetic anhydride; acetic acid;

With hydrogen; palladium on activated charcoal; In methanol; under 760 Torr;
DOI:10.1016/S0960-894X(02)00927-7

Reference yield:

: 64847-76-3
3-(hydroxyimino)methylbenzonitrile

: 544694-98-6
4-{4-[3-(3-carbamimidoyl-phenyl)-isoxazol-5-ylmethyl]-3-oxo-3,4-dihydro-2H-benzo[1,4]oxazin-7-yloxy}-piperidine-1-carboxylic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 6 steps

1.1: NCS / dimethylformamide

2.1: TEA

3.1: TsCl; pyridine

4.1: Cs₂CO₃ / dimethylformamide

5.1: NH₂OH / ethanol

6.1: acetic anhydride; acetic acid

6.2: H₂ / 10 percent Pd/C / methanol / 760 Torr

With pyridine; N-chloro-succinimide; TEA; hydroxylamine; acetic anhydride; caesium carbonate; acetic acid; p-toluenesulfonyl chloride; In ethanol; N,N-dimethyl-formamide;
DOI:10.1016/S0960-894X(02)00927-7

Reference yield:

: 24964-64-5
3-Cyanobenzaldehyde

: 544694-98-6
4-{4-[3-(3-carbamimidoyl-phenyl)-isoxazol-5-ylmethyl]-3-oxo-3,4-dihydro-2H-benzo[1,4]oxazin-7-yloxy}-piperidine-1-carboxylic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 7 steps

1.1: NH₂OH*HCl; TEA / ethanol

2.1: NCS / dimethylformamide

3.1: TEA

4.1: TsCl; pyridine

5.1: Cs₂CO₃ / dimethylformamide

6.1: NH₂OH / ethanol

7.1: acetic anhydride; acetic acid

7.2: H₂ / 10 percent Pd/C / methanol / 760 Torr

With pyridine; N-chloro-succinimide; TEA; hydroxylamine hydrochloride; hydroxylamine; acetic anhydride; caesium carbonate; acetic acid; p-toluenesulfonyl chloride; In ethanol; N,N-dimethyl-formamide;
DOI:10.1016/S0960-894X(02)00927-7