[(2-{2-[allyloxycarbonyl-(2-benzyloxycarbonylamino-ethyl)-amino]-acetylamino}-ethyl)-(2,2,2-trichloro-ethoxycarbonyl)-amino]-acetic acid

Base Information

Chemical Name:[(2-{2-[allyloxycarbonyl-(2-benzyloxycarbonylamino-ethyl)-amino]-acetylamino}-ethyl)-(2,2,2-trichloro-ethoxycarbonyl)-amino]-acetic acid
CAS No.:221554-85-4
Molecular Formula:C₂₃H₂₉Cl₃N₄O₉
Molecular Weight:611.864
Hs Code.:

Synonyms:[(2-{2-[allyloxycarbonyl-(2-benzyloxycarbonylamino-ethyl)-amino]-acetylamino}-ethyl)-(2,2,2-trichloro-ethoxycarbonyl)-amino]-acetic acid

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Chemical Property of [(2-{2-[allyloxycarbonyl-(2-benzyloxycarbonylamino-ethyl)-amino]-acetylamino}-ethyl)-(2,2,2-trichloro-ethoxycarbonyl)-amino]-acetic acid

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Technology Process of [(2-{2-[allyloxycarbonyl-(2-benzyloxycarbonylamino-ethyl)-amino]-acetylamino}-ethyl)-(2,2,2-trichloro-ethoxycarbonyl)-amino]-acetic acid

There total 2 articles about [(2-{2-[allyloxycarbonyl-(2-benzyloxycarbonylamino-ethyl)-amino]-acetylamino}-ethyl)-(2,2,2-trichloro-ethoxycarbonyl)-amino]-acetic 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: 90.0%

: 221554-83-2
[(2-{2-[allyloxycarbonyl-(2-benzyloxycarbonylamino-ethyl)-amino]-acetylamino}-ethyl)-(2,2,2-trichloro-ethoxycarbonyl)-amino]-acetic acid methyl ester

: 221554-85-4
[(2-{2-[allyloxycarbonyl-(2-benzyloxycarbonylamino-ethyl)-amino]-acetylamino}-ethyl)-(2,2,2-trichloro-ethoxycarbonyl)-amino]-acetic acid

Guidance literature:: With lithium hydroxide; In methanol; at 0 ℃; for 2h;
DOI:10.1016/S0040-4020(98)01211-3

Reference yield:

: 221554-80-9
N-<2-(N-Z)aminoethyl>-N-glycine

: 221554-85-4
[(2-{2-[allyloxycarbonyl-(2-benzyloxycarbonylamino-ethyl)-amino]-acetylamino}-ethyl)-(2,2,2-trichloro-ethoxycarbonyl)-amino]-acetic acid

Guidance literature:: Multi-step reaction with 2 steps

1: 1.) isobutyl chloroformate, 2.) Et₃N / 1.) CH₂Cl₂, -15 deg C, 15 min, 2.) CH₂Cl₂, -15 deg C (3 h), -> room temperature (1 h)

2: 90 percent / aq. LiOH / methanol / 2 h / 0 °C

With lithium hydroxide; triethylamine; isobutyl chloroformate; In methanol;
DOI:10.1016/S0040-4020(98)01211-3

Reference yield:

: 221554-85-4
[(2-{2-[allyloxycarbonyl-(2-benzyloxycarbonylamino-ethyl)-amino]-acetylamino}-ethyl)-(2,2,2-trichloro-ethoxycarbonyl)-amino]-acetic acid

: 221554-88-7
(allyloxycarbonyl-{2-[2-(2-{2-[allyloxycarbonyl-(2-benzyloxycarbonylamino-ethyl)-amino]-acetylamino}-ethylamino)-acetylamino]-ethyl}-amino)-acetic acid methyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 1.) isobutyl chloroformate, 2.) Et₃N / 1.) CH₂Cl₂, -15 deg C, 15 min, 2.) CH₂Cl₂, -15 deg C (3 h) -> room temperature (1 h)

2: 95 percent / Cd, AcOH / dimethylformamide / 2 h / Ambient temperature

With acetic acid; triethylamine; cadmium; isobutyl chloroformate; In N,N-dimethyl-formamide;
DOI:10.1016/S0040-4020(98)01211-3