5(S)-tert-butoxycarbonylamino-4(S)-hydroxy-7(S)-isopropyl-2(R)-methyl-8-[4-methoxy-3-(3-methoxypropyloxy)-phenyl]-octanoic acid N-(2-thiomorpholinoethyl) amide

Base Information

• Chemical Name: 5(S)-tert-butoxycarbonylamino-4(S)-hydroxy-7(S)-isopropyl-2(R)-methyl-8-[4-methoxy-3-(3-methoxypropyloxy)-phenyl]-octanoic acid N-(2-thiomorpholinoethyl) amide
• CAS No.: 173337-68-3
• Molecular Formula: C₃₄H₅₉N₃O₇S
• Molecular Weight: 653.924

Synonyms:5(S)-tert-butoxycarbonylamino-4(S)-hydroxy-7(S)-isopropyl-2(R)-methyl-8-[4-methoxy-3-(3-methoxypropyloxy)-phenyl]-octanoic acid N-(2-thiomorpholinoethyl) amide

Chemical Property of 5(S)-tert-butoxycarbonylamino-4(S)-hydroxy-7(S)-isopropyl-2(R)-methyl-8-[4-methoxy-3-(3-methoxypropyloxy)-phenyl]-octanoic acid N-(2-thiomorpholinoethyl) amide

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Technology Process of 5(S)-tert-butoxycarbonylamino-4(S)-hydroxy-7(S)-isopropyl-2(R)-methyl-8-[4-methoxy-3-(3-methoxypropyloxy)-phenyl]-octanoic acid N-(2-thiomorpholinoethyl) amide

There total 2 articles about 5(S)-tert-butoxycarbonylamino-4(S)-hydroxy-7(S)-isopropyl-2(R)-methyl-8-[4-methoxy-3-(3-methoxypropyloxy)-phenyl]-octanoic acid N-(2-thiomorpholinoethyl) amide 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-(2-Aminoethyl)thiomorpholine (53515-36-9) + (1S,3S,2'S,4'R)-[3-[4-methoxy-3-(3-methoxy-propoxy)-benzyl]-4-methyl-1-(4'-methyl-5-oxo-tetrahydro-furan-2'-yl)-pentyl]-carbamic acid tert-butyl ester (956035-15-7) → 5(S)-tert-butoxycarbonylamino-4(S)-hydroxy-7(S)-isopropyl-2(R)-methyl-8-[4-methoxy-3-(3-methoxypropyloxy)-phenyl]-octanoic acid N-(2-thiomorpholinoethyl) amide (173337-68-3)

Guidance literature:

at 80 ℃;

DOI:10.1021/jm070314y

Reference yield:

→ 5(S)-tert-butoxycarbonylamino-4(S)-hydroxy-7(S)-isopropyl-2(R)-methyl-8-[4-methoxy-3-(3-methoxypropyloxy)-phenyl]-octanoic acid N-(2-thiomorpholinoethyl) amide (173337-68-3)

Guidance literature:

Reference yield:

5(S)-tert-butoxycarbonylamino-4(S)-hydroxy-7(S)-isopropyl-2(R)-methyl-8-[4-methoxy-3-(3-methoxypropyloxy)-phenyl]-octanoic acid N-(2-thiomorpholinoethyl) amide (173337-68-3) → 5(S)-amino-4(S)-hydroxy-7(S)-isopropyl-2(R)-methyl-8-[4-methoxy-3-(3-methoxy-propyloxy)-phenyl]-octanoic acid N-(2-thiomorpholinoethyl)amide

Guidance literature:

With hydrogenchloride; In 1,4-dioxane; at 0 ℃;

DOI:10.1021/jm070314y

upstream raw materials:

4-(2-Aminoethyl)thiomorpholine

(1S,3S,2'S,4'R)-[3-[4-methoxy-3-(3-methoxy-propoxy)-benzyl]-4-methyl-1-(4'-methyl-5-oxo-tetrahydro-furan-2'-yl)-pentyl]-carbamic acid tert-butyl ester

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