tert-butyl ((1R)-2-{[4-formyl-1-(phenylsulfonyl)-1H-indol-5-yl]oxy}-1-methylethyl)carbamate

Base Information

Chemical Name:tert-butyl ((1R)-2-{[4-formyl-1-(phenylsulfonyl)-1H-indol-5-yl]oxy}-1-methylethyl)carbamate
CAS No.:1022954-68-2
Molecular Formula:C₂₃H₂₆N₂O₆S
Molecular Weight:458.535
Hs Code.:

Synonyms:tert-butyl ((1R)-2-{[4-formyl-1-(phenylsulfonyl)-1H-indol-5-yl]oxy}-1-methylethyl)carbamate

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Chemical Property of tert-butyl ((1R)-2-{[4-formyl-1-(phenylsulfonyl)-1H-indol-5-yl]oxy}-1-methylethyl)carbamate

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Technology Process of tert-butyl ((1R)-2-{[4-formyl-1-(phenylsulfonyl)-1H-indol-5-yl]oxy}-1-methylethyl)carbamate

There total 5 articles about tert-butyl ((1R)-2-{[4-formyl-1-(phenylsulfonyl)-1H-indol-5-yl]oxy}-1-methylethyl)carbamate 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:

: 1022953-36-1
5-hydroxy-1-(phenylsulfonyl)-1H-indole-4-carbaldehyde

: 79069-13-9,127516-56-7,147252-84-4,106391-86-0
(R)-2-tertbutoxycarbonylamino-1-propanol

: 1022954-68-2
tert-butyl ((1R)-2-{[4-formyl-1-(phenylsulfonyl)-1H-indol-5-yl]oxy}-1-methylethyl)carbamate

Guidance literature:: With diamide; triphenylphosphine; In dichloromethane; at 20 - 45 ℃; for 96h;

Reference yield:

: 1215-59-4
5-benzyloxy-1H-indole

: 1022954-68-2
tert-butyl ((1R)-2-{[4-formyl-1-(phenylsulfonyl)-1H-indol-5-yl]oxy}-1-methylethyl)carbamate

Guidance literature:: Multi-step reaction with 5 steps

1: sodium hydroxide; tetra(n-butyl)ammonium hydrogensulfate / dichloromethane; water / 20 °C

2: ammonium formate / palladium 10% on activated carbon / tetrahydrofuran; methanol / 20 °C

3: potassium hydroxide / methanol; water / 40 °C

4: manganese(IV) oxide / dichloromethane / 2 h / 20 °C

5: diamide; triphenylphosphine / dichloromethane / 96 h / 20 - 45 °C

With manganese(IV) oxide; potassium hydroxide; sodium hydroxide; diamide; ammonium formate; tetra(n-butyl)ammonium hydrogensulfate; triphenylphosphine; palladium 10% on activated carbon; In tetrahydrofuran; methanol; dichloromethane; water;

Reference yield:

: 98-09-9
benzenesulfonyl chloride

: 1022954-68-2
tert-butyl ((1R)-2-{[4-formyl-1-(phenylsulfonyl)-1H-indol-5-yl]oxy}-1-methylethyl)carbamate

Guidance literature:: Multi-step reaction with 5 steps

1: sodium hydroxide; tetra(n-butyl)ammonium hydrogensulfate / dichloromethane; water / 20 °C

2: ammonium formate / palladium 10% on activated carbon / tetrahydrofuran; methanol / 20 °C

3: potassium hydroxide / methanol; water / 40 °C

4: manganese(IV) oxide / dichloromethane / 2 h / 20 °C

5: diamide; triphenylphosphine / dichloromethane / 96 h / 20 - 45 °C

With manganese(IV) oxide; potassium hydroxide; sodium hydroxide; diamide; ammonium formate; tetra(n-butyl)ammonium hydrogensulfate; triphenylphosphine; palladium 10% on activated carbon; In tetrahydrofuran; methanol; dichloromethane; water;