(1S,3R,6S,8R)-11-methoxy-8-methoxymethyl-7,7,8-trimethyl-1-phenylaminomethyl-5-oxa-12-azadispiro[2.2.4.2]dodec-11-en-4-one

Base Information

Chemical Name:(1S,3R,6S,8R)-11-methoxy-8-methoxymethyl-7,7,8-trimethyl-1-phenylaminomethyl-5-oxa-12-azadispiro[2.2.4.2]dodec-11-en-4-one
CAS No.:244233-41-8
Molecular Formula:C₂₃H₃₂N₂O₄
Molecular Weight:400.518
Hs Code.:

Synonyms:(1S,3R,6S,8R)-11-methoxy-8-methoxymethyl-7,7,8-trimethyl-1-phenylaminomethyl-5-oxa-12-azadispiro[2.2.4.2]dodec-11-en-4-one

Suppliers and Price of (1S,3R,6S,8R)-11-methoxy-8-methoxymethyl-7,7,8-trimethyl-1-phenylaminomethyl-5-oxa-12-azadispiro[2.2.4.2]dodec-11-en-4-one

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 (1S,3R,6S,8R)-11-methoxy-8-methoxymethyl-7,7,8-trimethyl-1-phenylaminomethyl-5-oxa-12-azadispiro[2.2.4.2]dodec-11-en-4-one

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of (1S,3R,6S,8R)-11-methoxy-8-methoxymethyl-7,7,8-trimethyl-1-phenylaminomethyl-5-oxa-12-azadispiro[2.2.4.2]dodec-11-en-4-one

There total 15 articles about (1S,3R,6S,8R)-11-methoxy-8-methoxymethyl-7,7,8-trimethyl-1-phenylaminomethyl-5-oxa-12-azadispiro[2.2.4.2]dodec-11-en-4-one 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: 88.0%

: 62-53-3
aniline

: 244233-39-4
(1S,3R,6S,8R)-11-methoxy-8-methoxymethyl-7,7,8-trimethyl-4-oxo-5-oxa-12-azadispiro[2.2.4.2]dodec-11-en-1-carbaldehyde

: 244233-41-8
(1S,3R,6S,8R)-11-methoxy-8-methoxymethyl-7,7,8-trimethyl-1-phenylaminomethyl-5-oxa-12-azadispiro[2.2.4.2]dodec-11-en-4-one

Guidance literature:: With sodium cyanoborohydride; In tetrahydrofuran; at 20 ℃; for 1h;
DOI:10.1002/(SICI)1099-0690(199908)1999:8<1967::AID-EJOC1967>3.0.CO;2-G

Reference yield:

: 120697-88-3
(1S,3R)-1-hydroxy-3-methoxymethyl-2,2,3-trimethylcyclopentane-1-carboxylic acid

: 244233-41-8
(1S,3R,6S,8R)-11-methoxy-8-methoxymethyl-7,7,8-trimethyl-1-phenylaminomethyl-5-oxa-12-azadispiro[2.2.4.2]dodec-11-en-4-one

Guidance literature:: Multi-step reaction with 7 steps

1: tetrahydrofuran / 15 h / 20 °C

2: 88 percent / H₂ / Pd/C / ethanol / 15 h / 20 °C

3: 89 percent / 2-chloro-1-methylpyridinium iodide; diisopropylethylamine / CH₂Cl₂ / 8 h / Heating

4: 91 percent / CH₂Cl₂ / 16 h / 20 °C

5: 66 percent / NaN(SiMe₃)2 / tetrahydrofuran / 24 h / -10 °C

6: 89 percent / oxalyl chloride; DMSO; NEt₃ / CH₂Cl₂ / 0.25 h / -60 - 20 °C

7: 88 percent / NaBH₃CN / tetrahydrofuran / 1 h / 20 °C

With oxalyl dichloride; 2-chloro-1-methyl-pyridinium iodide; hydrogen; sodium hexamethyldisilazane; sodium cyanoborohydride; dimethyl sulfoxide; triethylamine; N-ethyl-N,N-diisopropylamine; palladium on activated charcoal; In tetrahydrofuran; ethanol; dichloromethane; 1: Acylation / 2: Hydrogenolysis / 3: Cyclization / 4: Methylation / 5: Metallation / 6: Swern oxidation / 7: Condensation;
DOI:10.1002/(SICI)1099-0690(199908)1999:8<1967::AID-EJOC1967>3.0.CO;2-G

Reference yield:

: C₁₅H₂₂N₂O₅

: 244233-41-8
(1S,3R,6S,8R)-11-methoxy-8-methoxymethyl-7,7,8-trimethyl-1-phenylaminomethyl-5-oxa-12-azadispiro[2.2.4.2]dodec-11-en-4-one

Guidance literature:: Multi-step reaction with 8 steps

1: tetrahydrofuran / 15 h / Heating

2: 84 percent / 24 h / 20 °C

3: 87 percent / NaN₃ / acetonitrile / 7 h / 70 °C

4: 85 percent / H₂ / Pd/C / tetrahydrofuran / 15 h / 20 °C

5: 91 percent / CH₂Cl₂ / 16 h / 20 °C

6: 66 percent / NaN(SiMe₃)2 / tetrahydrofuran / 24 h / -10 °C

7: 89 percent / oxalyl chloride; DMSO; NEt₃ / CH₂Cl₂ / 0.25 h / -60 - 20 °C

8: 88 percent / NaBH₃CN / tetrahydrofuran / 1 h / 20 °C

With sodium azide; oxalyl dichloride; hydrogen; sodium hexamethyldisilazane; sodium cyanoborohydride; dimethyl sulfoxide; triethylamine; palladium on activated charcoal; In tetrahydrofuran; dichloromethane; acetonitrile; 1: Esterification / 2: Acylation / 3: Substitution / 4: Hydrogenolysis / 5: Methylation / 6: Metallation / 7: Swern oxidation / 8: Condensation;
DOI:10.1002/(SICI)1099-0690(199908)1999:8<1967::AID-EJOC1967>3.0.CO;2-G