3-{[(R)-1-{[((S)-1-Carbamimidoyl-2-ethoxy-piperidin-3-ylcarbamoyl)-methyl]-carbamoyl}-2-(1-carbamimidoyl-piperidin-4-yl)-ethylsulfamoyl]-methyl}-benzoic acid

Base Information

Chemical Name:3-{[(R)-1-{[((S)-1-Carbamimidoyl-2-ethoxy-piperidin-3-ylcarbamoyl)-methyl]-carbamoyl}-2-(1-carbamimidoyl-piperidin-4-yl)-ethylsulfamoyl]-methyl}-benzoic acid
CAS No.:274928-61-9
Molecular Formula:C₂₇H₄₃N₉O₇S
Molecular Weight:637.761
Hs Code.:

3-{[(R)-1-{[((S)-1-Carbamimidoyl-2-ethoxy-piperidin-3-ylcarbamoyl)-methyl]-carbamoyl}-2-(1-carbamimidoyl-piperidin-4-yl)-ethylsulfamoyl]-methyl}-benzoic acid

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Chemical Property of 3-{[(R)-1-{[((S)-1-Carbamimidoyl-2-ethoxy-piperidin-3-ylcarbamoyl)-methyl]-carbamoyl}-2-(1-carbamimidoyl-piperidin-4-yl)-ethylsulfamoyl]-methyl}-benzoic acid

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Technology Process of 3-{[(R)-1-{[((S)-1-Carbamimidoyl-2-ethoxy-piperidin-3-ylcarbamoyl)-methyl]-carbamoyl}-2-(1-carbamimidoyl-piperidin-4-yl)-ethylsulfamoyl]-methyl}-benzoic acid

There total 8 articles about 3-{[(R)-1-{[((S)-1-Carbamimidoyl-2-ethoxy-piperidin-3-ylcarbamoyl)-methyl]-carbamoyl}-2-(1-carbamimidoyl-piperidin-4-yl)-ethylsulfamoyl]-methyl}-benzoic 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:

: 37535-58-3
(R)-2-(tert-butoxycarbonylamino)-3-(pyridin-4-yl)propanoic acid

: 274928-61-9
3-{[(R)-1-{[((S)-1-Carbamimidoyl-2-ethoxy-piperidin-3-ylcarbamoyl)-methyl]-carbamoyl}-2-(1-carbamimidoyl-piperidin-4-yl)-ethylsulfamoyl]-methyl}-benzoic acid

Guidance literature:: Multi-step reaction with 9 steps

1: 97 percent / EDC; HOBt; DIEA / acetonitrile

2: 100 percent / H₂; aq. AcOH / PtO₂ / ethanol

3: 55 percent / DIEA; THF / Heating

4: 100 percent / HCl / ethyl acetate

5: NMM / acetonitrile

6: 1N LiOH / ethanol

7: EDC; HOBt; NMM / acetonitrile

8: H₂ / 10 percent Pd/C / ethanol; acetic acid; H₂O

9: 1N LiOH / ethanol

With tetrahydrofuran; 4-methyl-morpholine; hydrogenchloride; lithium hydroxide; hydrogen; benzotriazol-1-ol; acetic acid; N-(3-dimethylaminopropyl)-N-ethylcarbodiimide; N-ethyl-N,N-diisopropylamine; platinum(IV) oxide; palladium on activated charcoal; In ethanol; water; acetic acid; ethyl acetate; acetonitrile; 1: coupling / 2: Hydrogenation / 3: guanylation / 4: deprotection / 5: Acylation / 6: Hydrolysis / 7: coupling / 8: Hydrogenolysis / 9: Hydrolysis;
DOI:10.1016/S0960-894X(00)00105-0

Reference yield:

: 274928-32-4
(2-tert-butoxycarbonylamino-3-pyridin-4-yl-propionylamino)-acetic acid methyl ester

: 274928-61-9
3-{[(R)-1-{[((S)-1-Carbamimidoyl-2-ethoxy-piperidin-3-ylcarbamoyl)-methyl]-carbamoyl}-2-(1-carbamimidoyl-piperidin-4-yl)-ethylsulfamoyl]-methyl}-benzoic acid

Guidance literature:: Multi-step reaction with 8 steps

1: 100 percent / H₂; aq. AcOH / PtO₂ / ethanol

2: 55 percent / DIEA; THF / Heating

3: 100 percent / HCl / ethyl acetate

4: NMM / acetonitrile

5: 1N LiOH / ethanol

6: EDC; HOBt; NMM / acetonitrile

7: H₂ / 10 percent Pd/C / ethanol; acetic acid; H₂O

8: 1N LiOH / ethanol

With tetrahydrofuran; 4-methyl-morpholine; hydrogenchloride; lithium hydroxide; hydrogen; benzotriazol-1-ol; acetic acid; N-(3-dimethylaminopropyl)-N-ethylcarbodiimide; N-ethyl-N,N-diisopropylamine; platinum(IV) oxide; palladium on activated charcoal; In ethanol; water; acetic acid; ethyl acetate; acetonitrile; 1: Hydrogenation / 2: guanylation / 3: deprotection / 4: Acylation / 5: Hydrolysis / 6: coupling / 7: Hydrogenolysis / 8: Hydrolysis;
DOI:10.1016/S0960-894X(00)00105-0

Reference yield:

: 274928-33-5
(2-tert-butoxycarbonylamino-3-piperidin-4-yl-propionylamino)-acetic acid methyl ester

: 274928-61-9
3-{[(R)-1-{[((S)-1-Carbamimidoyl-2-ethoxy-piperidin-3-ylcarbamoyl)-methyl]-carbamoyl}-2-(1-carbamimidoyl-piperidin-4-yl)-ethylsulfamoyl]-methyl}-benzoic acid

Guidance literature:: Multi-step reaction with 7 steps

1: 55 percent / DIEA; THF / Heating

2: 100 percent / HCl / ethyl acetate

3: NMM / acetonitrile

4: 1N LiOH / ethanol

5: EDC; HOBt; NMM / acetonitrile

6: H₂ / 10 percent Pd/C / ethanol; acetic acid; H₂O

7: 1N LiOH / ethanol

With tetrahydrofuran; 4-methyl-morpholine; hydrogenchloride; lithium hydroxide; hydrogen; benzotriazol-1-ol; N-(3-dimethylaminopropyl)-N-ethylcarbodiimide; N-ethyl-N,N-diisopropylamine; palladium on activated charcoal; In ethanol; water; acetic acid; ethyl acetate; acetonitrile; 1: guanylation / 2: deprotection / 3: Acylation / 4: Hydrolysis / 5: coupling / 6: Hydrogenolysis / 7: Hydrolysis;
DOI:10.1016/S0960-894X(00)00105-0