2-[(4-Acetylamino-2-ethoxy-3-hydroxy-benzoylamino)-methyl]-morpholine-4-carboxylic acid tert-butyl ester

Base Information

Chemical Name:2-[(4-Acetylamino-2-ethoxy-3-hydroxy-benzoylamino)-methyl]-morpholine-4-carboxylic acid tert-butyl ester
CAS No.:182068-15-1
Molecular Formula:C₂₁H₃₁N₃O₇
Molecular Weight:437.493
Hs Code.:

Synonyms:2-[(4-Acetylamino-2-ethoxy-3-hydroxy-benzoylamino)-methyl]-morpholine-4-carboxylic acid tert-butyl ester

Suppliers and Price of 2-[(4-Acetylamino-2-ethoxy-3-hydroxy-benzoylamino)-methyl]-morpholine-4-carboxylic acid tert-butyl ester

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of 2-[(4-Acetylamino-2-ethoxy-3-hydroxy-benzoylamino)-methyl]-morpholine-4-carboxylic acid tert-butyl ester

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of 2-[(4-Acetylamino-2-ethoxy-3-hydroxy-benzoylamino)-methyl]-morpholine-4-carboxylic acid tert-butyl ester

There total 10 articles about 2-[(4-Acetylamino-2-ethoxy-3-hydroxy-benzoylamino)-methyl]-morpholine-4-carboxylic acid tert-butyl 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: 97.0%

: 108-24-7
acetic anhydride

: 182068-12-8
2-[(2-Ethoxy-3-hydroxy-4-nitro-benzoylamino)-methyl]-morpholine-4-carboxylic acid tert-butyl ester

: 182068-15-1
2-[(4-Acetylamino-2-ethoxy-3-hydroxy-benzoylamino)-methyl]-morpholine-4-carboxylic acid tert-butyl ester

Guidance literature:: With hydrogen; palladium on activated charcoal; In ethanol; for 6h; under 1900 Torr; Ambient temperature;
DOI:10.1248/cpb.44.1484

Reference yield:

: 24677-78-9
2,3-dihydroxybenzaldehyde

: 182068-15-1
2-[(4-Acetylamino-2-ethoxy-3-hydroxy-benzoylamino)-methyl]-morpholine-4-carboxylic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 9 steps

1: 1.) NaH, DMSO / 1.) 110 deg C, 2 h, 2.) RT, 18 h

2: 22 percent / 70percent aq. HNO₃, AcOH / toluene / 0.08 h / 5 - 10 °C

3: 77 percent / AgNO₃, 1N aq. NaOH / methanol / 6 h / 85 °C

4: SOCl₂, DMF / CH₂Cl₂ / 1.5 h / Heating

5: Et₃N / CH₂Cl₂ / Ambient temperature

6: toluene / 10 h / Heating

7: MeOH / 2 h / Heating

8: Et₃N / methanol / 18 h / Ambient temperature

9: 97 percent / H₂ / 10percent Pd/C / ethanol / 6 h / 1900 Torr / Ambient temperature

With methanol; sodium hydroxide; thionyl chloride; hydrogen; nitric acid; sodium hydride; silver nitrate; acetic acid; dimethyl sulfoxide; triethylamine; N,N-dimethyl-formamide; palladium on activated charcoal; In methanol; ethanol; dichloromethane; toluene;
DOI:10.1248/cpb.44.1484

Reference yield:

: 112914-13-3
2-aminomethyl-4-(4-fluoro-benzyl) morpholine

: 182068-15-1
2-[(4-Acetylamino-2-ethoxy-3-hydroxy-benzoylamino)-methyl]-morpholine-4-carboxylic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 5 steps

1: Et₃N / CH₂Cl₂ / Ambient temperature

2: toluene / 10 h / Heating

3: MeOH / 2 h / Heating

4: Et₃N / methanol / 18 h / Ambient temperature

5: 97 percent / H₂ / 10percent Pd/C / ethanol / 6 h / 1900 Torr / Ambient temperature

With methanol; hydrogen; triethylamine; palladium on activated charcoal; In methanol; ethanol; dichloromethane; toluene;
DOI:10.1248/cpb.44.1484