(S)-4-{3-[3-(5-tert-butoxycarbonylmethyl-4-oxo-2,3,4,5-tetrahydro-1,5-benzothiazepin-3-yl)ureido]benzyloxycarbonylamino}butyric acid methyl ester

Base Information

Chemical Name:(S)-4-{3-[3-(5-tert-butoxycarbonylmethyl-4-oxo-2,3,4,5-tetrahydro-1,5-benzothiazepin-3-yl)ureido]benzyloxycarbonylamino}butyric acid methyl ester
CAS No.:195621-81-9
Molecular Formula:C₂₉H₃₆N₄O₈S
Molecular Weight:600.693
Hs Code.:

(S)-4-{3-[3-(5-tert-butoxycarbonylmethyl-4-oxo-2,3,4,5-tetrahydro-1,5-benzothiazepin-3-yl)ureido]benzyloxycarbonylamino}butyric acid methyl ester

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Chemical Property of (S)-4-{3-[3-(5-tert-butoxycarbonylmethyl-4-oxo-2,3,4,5-tetrahydro-1,5-benzothiazepin-3-yl)ureido]benzyloxycarbonylamino}butyric acid methyl ester

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Technology Process of (S)-4-{3-[3-(5-tert-butoxycarbonylmethyl-4-oxo-2,3,4,5-tetrahydro-1,5-benzothiazepin-3-yl)ureido]benzyloxycarbonylamino}butyric acid methyl ester

There total 6 articles about (S)-4-{3-[3-(5-tert-butoxycarbonylmethyl-4-oxo-2,3,4,5-tetrahydro-1,5-benzothiazepin-3-yl)ureido]benzyloxycarbonylamino}butyric acid methyl 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:

: 1493-27-2,127723-77-7
ortho-nitrofluorobenzene

: 195621-81-9
(S)-4-{3-[3-(5-tert-butoxycarbonylmethyl-4-oxo-2,3,4,5-tetrahydro-1,5-benzothiazepin-3-yl)ureido]benzyloxycarbonylamino}butyric acid methyl ester

Guidance literature:: Multi-step reaction with 7 steps

1: 96 percent / t-BuOK / H₂O; methanol / 2 h / Ambient temperature

2: Na₂CO₃

3: H₂ / Pd/C

4: NCPO(OEt)2

5: H₂NNH₂*H₂O / ethanol / 1 h / Heating

6: Et₃N / CH₂Cl₂ / 2 h / Heating

7: KOH, TBAB / tetrahydrofuran / 2 h / Ambient temperature

With potassium hydroxide; Diethy phosphocyanidate; potassium tert-butylate; tetrabutylammomium bromide; hydrogen; sodium carbonate; hydrazine hydrate; triethylamine; palladium on activated charcoal; In tetrahydrofuran; methanol; ethanol; dichloromethane; water;
DOI:10.1016/S0968-0896(97)00075-8

Reference yield:

: 105593-48-4
amino-(2-nitrophenylsulfanyl)acetic acid

: 195621-81-9
(S)-4-{3-[3-(5-tert-butoxycarbonylmethyl-4-oxo-2,3,4,5-tetrahydro-1,5-benzothiazepin-3-yl)ureido]benzyloxycarbonylamino}butyric acid methyl ester

Guidance literature:: Multi-step reaction with 6 steps

1: Na₂CO₃

2: H₂ / Pd/C

3: NCPO(OEt)2

4: H₂NNH₂*H₂O / ethanol / 1 h / Heating

5: Et₃N / CH₂Cl₂ / 2 h / Heating

6: KOH, TBAB / tetrahydrofuran / 2 h / Ambient temperature

With potassium hydroxide; Diethy phosphocyanidate; tetrabutylammomium bromide; hydrogen; sodium carbonate; hydrazine hydrate; triethylamine; palladium on activated charcoal; In tetrahydrofuran; ethanol; dichloromethane;
DOI:10.1016/S0968-0896(97)00075-8

Reference yield:

: 105593-49-5
(S)-3-phtalimido-2,3-dihydro-1,5(5H)-benzothiazepin-4-one

: 195621-81-9
(S)-4-{3-[3-(5-tert-butoxycarbonylmethyl-4-oxo-2,3,4,5-tetrahydro-1,5-benzothiazepin-3-yl)ureido]benzyloxycarbonylamino}butyric acid methyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: H₂NNH₂*H₂O / ethanol / 1 h / Heating

2: Et₃N / CH₂Cl₂ / 2 h / Heating

3: KOH, TBAB / tetrahydrofuran / 2 h / Ambient temperature

With potassium hydroxide; tetrabutylammomium bromide; hydrazine hydrate; triethylamine; In tetrahydrofuran; ethanol; dichloromethane;
DOI:10.1016/S0968-0896(97)00075-8