2-Benzoylamino-thiopropionic acid S-[(2R,3R)-3-(2-benzyloxycarbonylamino-acetylsulfanylmethyl)-1,4,7,10,13,16-hexaoxa-cyclooctadec-2-ylmethyl] ester

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Chemical Name:2-Benzoylamino-thiopropionic acid S-[(2R,3R)-3-(2-benzyloxycarbonylamino-acetylsulfanylmethyl)-1,4,7,10,13,16-hexaoxa-cyclooctadec-2-ylmethyl] ester
CAS No.:125372-70-5
Molecular Formula:C₃₄H₄₆N₂O₁₁S₂
Molecular Weight:722.878
Hs Code.:

2-Benzoylamino-thiopropionic acid S-[(2R,3R)-3-(2-benzyloxycarbonylamino-acetylsulfanylmethyl)-1,4,7,10,13,16-hexaoxa-cyclooctadec-2-ylmethyl] ester

Synonyms:2-Benzoylamino-thiopropionic acid S-[(2R,3R)-3-(2-benzyloxycarbonylamino-acetylsulfanylmethyl)-1,4,7,10,13,16-hexaoxa-cyclooctadec-2-ylmethyl] ester

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Chemical Property of 2-Benzoylamino-thiopropionic acid S-[(2R,3R)-3-(2-benzyloxycarbonylamino-acetylsulfanylmethyl)-1,4,7,10,13,16-hexaoxa-cyclooctadec-2-ylmethyl] ester

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Technology Process of 2-Benzoylamino-thiopropionic acid S-[(2R,3R)-3-(2-benzyloxycarbonylamino-acetylsulfanylmethyl)-1,4,7,10,13,16-hexaoxa-cyclooctadec-2-ylmethyl] ester

There total 3 articles about 2-Benzoylamino-thiopropionic acid S-[(2R,3R)-3-(2-benzyloxycarbonylamino-acetylsulfanylmethyl)-1,4,7,10,13,16-hexaoxa-cyclooctadec-2-ylmethyl] 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: 80.0%

: 98-88-4
benzoyl chloride

: 125412-50-2
(2S,3S)-S-(N-carbobenzyloxyglycyl)-S'-L-alanyl-2,3-bis(mercaptomethyl)-1,4,7,10,13,16-hexaoxacyclooctadecane hydrochloride

: 125372-70-5
2-Benzoylamino-thiopropionic acid S-[(2R,3R)-3-(2-benzyloxycarbonylamino-acetylsulfanylmethyl)-1,4,7,10,13,16-hexaoxa-cyclooctadec-2-ylmethyl] ester

Guidance literature:: With TEA; In chloroform; for 0.5h; Ambient temperature;
DOI:10.1248/cpb.37.912

Reference yield:

: 67654-51-7
(-)-(2R,3R)-2,3-bis(mercaptomethyl)-1,4,7,10,13,16-hexaoxacyclooctadecane

: 125372-70-5
2-Benzoylamino-thiopropionic acid S-[(2R,3R)-3-(2-benzyloxycarbonylamino-acetylsulfanylmethyl)-1,4,7,10,13,16-hexaoxa-cyclooctadec-2-ylmethyl] ester

Guidance literature:: Multi-step reaction with 2 steps

1: 1.) Et₃N, diethyl pyrocarbonate 2.) pyridine / 1.) DMF, 0 deg C, 1 h, then room t., 1 h, 2.) acetone, room t., 20 min

2: 80 percent / TEA / CHCl₃ / 0.5 h / Ambient temperature

With pyridine; TEA; triethylamine; diethyl dicarbonate; In chloroform;
DOI:10.1248/cpb.37.912

Reference yield:

: 1138-80-3
N-(Benzyloxycarbonyl)glycine

: 125372-70-5
2-Benzoylamino-thiopropionic acid S-[(2R,3R)-3-(2-benzyloxycarbonylamino-acetylsulfanylmethyl)-1,4,7,10,13,16-hexaoxa-cyclooctadec-2-ylmethyl] ester

Guidance literature:: Multi-step reaction with 2 steps

1: 1.) Et₃N, diethyl pyrocarbonate 2.) pyridine / 1.) DMF, 0 deg C, 1 h, then room t., 1 h, 2.) acetone, room t., 20 min

2: 80 percent / TEA / CHCl₃ / 0.5 h / Ambient temperature

With pyridine; TEA; triethylamine; diethyl dicarbonate; In chloroform;
DOI:10.1248/cpb.37.912