2-benzyloxycarbonylamino-3-(tert-butyl-dimethyl-silanyloxy)-3-[1-(1,1-dimethyl-2-oxo-ethyl)-1H-indol-3-yl]-propionic acid ethyl ester

Base Information

Chemical Name:2-benzyloxycarbonylamino-3-(tert-butyl-dimethyl-silanyloxy)-3-[1-(1,1-dimethyl-2-oxo-ethyl)-1H-indol-3-yl]-propionic acid ethyl ester
CAS No.:753488-09-4
Molecular Formula:C₃₁H₄₂N₂O₆Si
Molecular Weight:566.77
Hs Code.:

2-benzyloxycarbonylamino-3-(<i>tert</i>-butyl-dimethyl-silanyloxy)-3-[1-(1,1-dimethyl-2-oxo-ethyl)-1<i>H</i>-indol-3-yl]-propionic acid ethyl ester

Synonyms:2-benzyloxycarbonylamino-3-(tert-butyl-dimethyl-silanyloxy)-3-[1-(1,1-dimethyl-2-oxo-ethyl)-1H-indol-3-yl]-propionic acid ethyl ester

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Chemical Property of 2-benzyloxycarbonylamino-3-(tert-butyl-dimethyl-silanyloxy)-3-[1-(1,1-dimethyl-2-oxo-ethyl)-1H-indol-3-yl]-propionic acid ethyl ester

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Technology Process of 2-benzyloxycarbonylamino-3-(tert-butyl-dimethyl-silanyloxy)-3-[1-(1,1-dimethyl-2-oxo-ethyl)-1H-indol-3-yl]-propionic acid ethyl ester

There total 6 articles about 2-benzyloxycarbonylamino-3-(tert-butyl-dimethyl-silanyloxy)-3-[1-(1,1-dimethyl-2-oxo-ethyl)-1H-indol-3-yl]-propionic 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: 87.0%

: 753487-69-3
2-benzyloxycarbonylamino-3-(tert-butyl-dimethyl-silanyloxy)-3-[1-(2-hydroxy-1,1-dimethyl-ethyl)-1H-indol-3-yl]-propionic acid ethyl ester

: 753488-09-4
2-benzyloxycarbonylamino-3-(tert-butyl-dimethyl-silanyloxy)-3-[1-(1,1-dimethyl-2-oxo-ethyl)-1H-indol-3-yl]-propionic acid ethyl ester

Guidance literature:: With oxalyl dichloride; dimethyl sulfoxide; N-ethyl-N,N-diisopropylamine; In dichloromethane; at -78 - 20 ℃;
DOI:10.1021/ol049065n

Reference yield:

: acetic acid 2-indol-1-yl-2-methyl-propyl ester

: 753488-09-4
2-benzyloxycarbonylamino-3-(tert-butyl-dimethyl-silanyloxy)-3-[1-(1,1-dimethyl-2-oxo-ethyl)-1H-indol-3-yl]-propionic acid ethyl ester

Guidance literature:: Multi-step reaction with 6 steps

1.1: POCl₃ / 0.5 h / 0 °C

1.2: 90 percent / 1.5 h / 20 °C

2.1: NaH / tetrahydrofuran / 1 h / 20 °C

2.2: 90 percent / tetrahydrofuran / 8 h / 20 °C

3.1: NaOH; K₂[OsO₂(OH)4]; t-butyl hypochlorite / propan-1-ol; H₂O / 0.42 h

3.2: (DHQD)2AQH; K₂[OsO₂(OH)4] / propan-1-ol; H₂O / 3 h

4.1: 97 percent / i-Pr₂NEt / CH₂Cl₂ / -78 - 20 °C

5.1: 97 percent / K₂CO₃ / methanol / 2 h / 0 °C

6.1: 87 percent / DMSO; (COCl)2; i-Pr₂NEt / CH₂Cl₂ / -78 - 20 °C

With sodium hydroxide; oxalyl dichloride; tert-butylhypochlorite; K2; sodium hydride; potassium carbonate; dimethyl sulfoxide; N-ethyl-N,N-diisopropylamine; trichlorophosphate; In tetrahydrofuran; methanol; propan-1-ol; dichloromethane; water; 2.2: Wittig reaction / 3.2: Sharpless asymmetric aminohydroxylation / 6.1: Swern oxidation;
DOI:10.1021/ol049065n

Reference yield:

: 753488-05-0
acetic acid 2-(3-formyl-indol-1-yl)-2-methyl-propyl ester

: 753488-09-4
2-benzyloxycarbonylamino-3-(tert-butyl-dimethyl-silanyloxy)-3-[1-(1,1-dimethyl-2-oxo-ethyl)-1H-indol-3-yl]-propionic acid ethyl ester

Guidance literature:: Multi-step reaction with 5 steps

1.1: NaH / tetrahydrofuran / 1 h / 20 °C

1.2: 90 percent / tetrahydrofuran / 8 h / 20 °C

2.1: NaOH; K₂[OsO₂(OH)4]; t-butyl hypochlorite / propan-1-ol; H₂O / 0.42 h

2.2: (DHQD)2AQH; K₂[OsO₂(OH)4] / propan-1-ol; H₂O / 3 h

3.1: 97 percent / i-Pr₂NEt / CH₂Cl₂ / -78 - 20 °C

4.1: 97 percent / K₂CO₃ / methanol / 2 h / 0 °C

5.1: 87 percent / DMSO; (COCl)2; i-Pr₂NEt / CH₂Cl₂ / -78 - 20 °C

With sodium hydroxide; oxalyl dichloride; tert-butylhypochlorite; K2; sodium hydride; potassium carbonate; dimethyl sulfoxide; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; methanol; propan-1-ol; dichloromethane; water; 1.2: Wittig reaction / 2.2: Sharpless asymmetric aminohydroxylation / 5.1: Swern oxidation;
DOI:10.1021/ol049065n