2-(2-{3-acetylamino-2-benzyloxy-6-benzyloxymethyl-5-[4,5-diacetoxy-6-acetoxymethyl-3-(2,2,2-trichloro-ethoxycarbonylamino)-tetrahydro-pyran-2-yloxy]-tetrahydro-pyran-4-yloxy}-propionylamino)-propionic acid 2-benzenesulfonyl-ethyl ester

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Chemical Name:2-(2-{3-acetylamino-2-benzyloxy-6-benzyloxymethyl-5-[4,5-diacetoxy-6-acetoxymethyl-3-(2,2,2-trichloro-ethoxycarbonylamino)-tetrahydro-pyran-2-yloxy]-tetrahydro-pyran-4-yloxy}-propionylamino)-propionic acid 2-benzenesulfonyl-ethyl ester
CAS No.:367276-20-8
Molecular Formula:C₅₁H₆₂Cl₃N₃O₂₀S
Molecular Weight:1175.49
Hs Code.:

2-(2-{3-acetylamino-2-benzyloxy-6-benzyloxymethyl-5-[4,5-diacetoxy-6-acetoxymethyl-3-(2,2,2-trichloro-ethoxycarbonylamino)-tetrahydro-pyran-2-yloxy]-tetrahydro-pyran-4-yloxy}-propionylamino)-propionic acid 2-benzenesulfonyl-ethyl ester

Synonyms:2-(2-{3-acetylamino-2-benzyloxy-6-benzyloxymethyl-5-[4,5-diacetoxy-6-acetoxymethyl-3-(2,2,2-trichloro-ethoxycarbonylamino)-tetrahydro-pyran-2-yloxy]-tetrahydro-pyran-4-yloxy}-propionylamino)-propionic acid 2-benzenesulfonyl-ethyl ester

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Chemical Property of 2-(2-{3-acetylamino-2-benzyloxy-6-benzyloxymethyl-5-[4,5-diacetoxy-6-acetoxymethyl-3-(2,2,2-trichloro-ethoxycarbonylamino)-tetrahydro-pyran-2-yloxy]-tetrahydro-pyran-4-yloxy}-propionylamino)-propionic acid 2-benzenesulfonyl-ethyl ester

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Technology Process of 2-(2-{3-acetylamino-2-benzyloxy-6-benzyloxymethyl-5-[4,5-diacetoxy-6-acetoxymethyl-3-(2,2,2-trichloro-ethoxycarbonylamino)-tetrahydro-pyran-2-yloxy]-tetrahydro-pyran-4-yloxy}-propionylamino)-propionic acid 2-benzenesulfonyl-ethyl ester

There total 5 articles about 2-(2-{3-acetylamino-2-benzyloxy-6-benzyloxymethyl-5-[4,5-diacetoxy-6-acetoxymethyl-3-(2,2,2-trichloro-ethoxycarbonylamino)-tetrahydro-pyran-2-yloxy]-tetrahydro-pyran-4-yloxy}-propionylamino)-propionic acid 2-benzenesulfonyl-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: 84.0%

: 67124-60-1
3,4,6-Tri-O-acetyl-2-deoxy-2-(2,2,2-trichloroethoxycarbonylamino)-α-D-glucopyranosyl bromide

: 367276-19-5
(S)-2-[(R)-2-((2S,3R,4R,5S,6R)-3-Acetylamino-2-benzyloxy-6-benzyloxymethyl-5-hydroxy-tetrahydro-pyran-4-yloxy)-propionylamino]-propionic acid 2-benzenesulfonyl-ethyl ester

: 367276-20-8
2-(2-{3-acetylamino-2-benzyloxy-6-benzyloxymethyl-5-[4,5-diacetoxy-6-acetoxymethyl-3-(2,2,2-trichloro-ethoxycarbonylamino)-tetrahydro-pyran-2-yloxy]-tetrahydro-pyran-4-yloxy}-propionylamino)-propionic acid 2-benzenesulfonyl-ethyl ester

Guidance literature:: With 4 A molecular sieve; silver trifluoromethanesulfonate; In dichloromethane; at 20 ℃;
DOI:10.1021/ol016692t

Reference yield: 50.0%

: 3,4,6-tri-O-acetyl-2-deoxy-2-(2,2,2-trichloroethoxycarbonylamino)-D-glucopyranosyl trichloroacetimidate

: 367276-19-5
(S)-2-[(R)-2-((2S,3R,4R,5S,6R)-3-Acetylamino-2-benzyloxy-6-benzyloxymethyl-5-hydroxy-tetrahydro-pyran-4-yloxy)-propionylamino]-propionic acid 2-benzenesulfonyl-ethyl ester

: 367276-20-8
2-(2-{3-acetylamino-2-benzyloxy-6-benzyloxymethyl-5-[4,5-diacetoxy-6-acetoxymethyl-3-(2,2,2-trichloro-ethoxycarbonylamino)-tetrahydro-pyran-2-yloxy]-tetrahydro-pyran-4-yloxy}-propionylamino)-propionic acid 2-benzenesulfonyl-ethyl ester

Guidance literature:: With trimethylsilyl trifluoromethanesulfonate; In dichloromethane; at 0 ℃; for 3h; Molecular sieve;
DOI:10.1002/chem.201400307

Reference yield:

: 73089-68-6
benzyl 2-acetamido-4,6-O-benzylidene-3-O-[(R)-1-carboxyethyl]-2-deoxy-α-D-glucopyranoside

: 367276-20-8
2-(2-{3-acetylamino-2-benzyloxy-6-benzyloxymethyl-5-[4,5-diacetoxy-6-acetoxymethyl-3-(2,2,2-trichloro-ethoxycarbonylamino)-tetrahydro-pyran-2-yloxy]-tetrahydro-pyran-4-yloxy}-propionylamino)-propionic acid 2-benzenesulfonyl-ethyl ester

Guidance literature:: Multi-step reaction with 3 steps

1.1: N-methylmorpholine; 2-chloro-4,6-dimethoxy-1,3,5-triazine / CH₂Cl₂ / 0.75 h / 0 °C

1.2: 95 percent / N-methylmorpholine / CH₂Cl₂ / 72 h / 20 °C

2.1: 61 percent / Et₃SiH; TFA / CH₂Cl₂ / 0 °C

3.1: 84 percent / AgOTf; molecular sieves 4 Angstroem / CH₂Cl₂ / 20 °C

With 4-methyl-morpholine; triethylsilane; 2-chloro-4,6-dimethoxy-1 ,3,5-triazine; 4 A molecular sieve; silver trifluoromethanesulfonate; trifluoroacetic acid; In dichloromethane;
DOI:10.1021/ol016692t