2-[(adamantan-1-yloxy)-(1-benzyloxycarbonylamino-2-phenyl-ethyl)-phosphinoylmethyl]-5-phenyl-pentanoic acid ethyl ester

Base Information

• Chemical Name: 2-[(adamantan-1-yloxy)-(1-benzyloxycarbonylamino-2-phenyl-ethyl)-phosphinoylmethyl]-5-phenyl-pentanoic acid ethyl ester
• CAS No.: 237394-38-6
• Molecular Formula: C₄₀H₅₀NO₆P
• Molecular Weight: 671.814

Synonyms:2-[(adamantan-1-yloxy)-(1-benzyloxycarbonylamino-2-phenyl-ethyl)-phosphinoylmethyl]-5-phenyl-pentanoic acid ethyl ester

Chemical Property of 2-[(adamantan-1-yloxy)-(1-benzyloxycarbonylamino-2-phenyl-ethyl)-phosphinoylmethyl]-5-phenyl-pentanoic acid ethyl ester

Chemical Property:

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Technology Process of 2-[(adamantan-1-yloxy)-(1-benzyloxycarbonylamino-2-phenyl-ethyl)-phosphinoylmethyl]-5-phenyl-pentanoic acid ethyl ester

There total 3 articles about 2-[(adamantan-1-yloxy)-(1-benzyloxycarbonylamino-2-phenyl-ethyl)-phosphinoylmethyl]-5-phenyl-pentanoic acid ethyl 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: 75.0%

1-Adamantyl bromide (768-90-1) + 2-[(1-benzyloxycarbonylamino-2-phenyl-ethyl)-hydroxy-phosphinoylmethyl]-5-phenyl-pentanoic acid ethyl ester (237394-24-0) → 2-[(adamantan-1-yloxy)-(1-benzyloxycarbonylamino-2-phenyl-ethyl)-phosphinoylmethyl]-5-phenyl-pentanoic acid ethyl ester (237394-38-6)

Guidance literature:

With silver(l) oxide; In chloroform; for 0.5h; Heating;

DOI:10.1021/jm9900164

Reference yield:

ethyl 2-methylene-5-phenylpentanoate (27356-88-3) → 2-[(adamantan-1-yloxy)-(1-benzyloxycarbonylamino-2-phenyl-ethyl)-phosphinoylmethyl]-5-phenyl-pentanoic acid ethyl ester (237394-38-6)

Guidance literature:

Multi-step reaction with 2 steps

1: 1.) hexamethyldisilazane / 1.) 110 deg C, 1 h, 2.) 110 deg C, 3 h

2: 75 percent / silver oxide / CHCl₃ / 0.5 h / Heating

With 1,1,1,3,3,3-hexamethyl-disilazane; silver(l) oxide; In chloroform;

DOI:10.1021/jm9900164

Reference yield:

[2-phenyl-1-[[(phenylmethoxy)carbonyl]amino]ethyl]phosphinic acid (115961-49-4) → 2-[(adamantan-1-yloxy)-(1-benzyloxycarbonylamino-2-phenyl-ethyl)-phosphinoylmethyl]-5-phenyl-pentanoic acid ethyl ester (237394-38-6)

Guidance literature:

Multi-step reaction with 2 steps

1: 1.) hexamethyldisilazane / 1.) 110 deg C, 1 h, 2.) 110 deg C, 3 h

2: 75 percent / silver oxide / CHCl₃ / 0.5 h / Heating

With 1,1,1,3,3,3-hexamethyl-disilazane; silver(l) oxide; In chloroform;

DOI:10.1021/jm9900164

upstream raw materials:

1-Adamantyl bromide

2-[(1-benzyloxycarbonylamino-2-phenyl-ethyl)-hydroxy-phosphinoylmethyl]-5-phenyl-pentanoic acid ethyl ester

ethyl 2-methylene-5-phenylpentanoate

[2-phenyl-1-[[(phenylmethoxy)carbonyl]amino]ethyl]phosphinic acid

Downstream raw materials:

2-[(adamantan-1-yloxy)-(1-benzyloxycarbonylamino-2-phenyl-ethyl)-phosphinoylmethyl]-5-phenyl-pentanoic acid

2-{(adamantan-1-yloxy)-[1-(9H-fluoren-9-ylmethoxycarbonylamino)-2-phenyl-ethyl]-phosphinoylmethyl}-5-phenyl-pentanoic acid

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