(2R,6S)-2-tert-Butyl-6-isobutyl-4-methoxy-5,6-dihydro-2H-pyrimidine-1-carboxylic acid benzyl ester

Base Information

Chemical Name:(2R,6S)-2-tert-Butyl-6-isobutyl-4-methoxy-5,6-dihydro-2H-pyrimidine-1-carboxylic acid benzyl ester
CAS No.:220116-88-1
Molecular Formula:C₂₁H₃₂N₂O₃
Molecular Weight:360.497
Hs Code.:

Synonyms:(2R,6S)-2-tert-Butyl-6-isobutyl-4-methoxy-5,6-dihydro-2H-pyrimidine-1-carboxylic acid benzyl ester

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Chemical Property of (2R,6S)-2-tert-Butyl-6-isobutyl-4-methoxy-5,6-dihydro-2H-pyrimidine-1-carboxylic acid benzyl ester

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Technology Process of (2R,6S)-2-tert-Butyl-6-isobutyl-4-methoxy-5,6-dihydro-2H-pyrimidine-1-carboxylic acid benzyl ester

There total 1 articles about (2R,6S)-2-tert-Butyl-6-isobutyl-4-methoxy-5,6-dihydro-2H-pyrimidine-1-carboxylic acid benzyl 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: 64.0%

: 420-37-1
trimethoxonium tetrafluoroborate

: 220116-78-9
(2R,6S)-2-tert-Butyl-6-isobutyl-4-oxo-tetrahydro-pyrimidine-1-carboxylic acid benzyl ester

: 220116-88-1
(2R,6S)-2-tert-Butyl-6-isobutyl-4-methoxy-5,6-dihydro-2H-pyrimidine-1-carboxylic acid benzyl ester

Guidance literature:: In dichloromethane; at 0 ℃; for 12h;
DOI:10.1002/(SICI)1099-0690(199901)1999:1<335::AID-EJOC335>3.0.CO;2-A

Reference yield: 78.0%

: 100-39-0
benzyl bromide

: 220116-88-1
(2R,6S)-2-tert-Butyl-6-isobutyl-4-methoxy-5,6-dihydro-2H-pyrimidine-1-carboxylic acid benzyl ester

: 220117-16-8
(2R,5S,6S)-5-Benzyl-2-tert-butyl-6-isobutyl-4-methoxy-5,6-dihydro-2H-pyrimidine-1-carboxylic acid benzyl ester

Guidance literature:: With lithium diisopropyl amide; In tetrahydrofuran; at -78 - -30 ℃; for 6h;
DOI:10.1002/(SICI)1099-0690(199901)1999:1<335::AID-EJOC335>3.0.CO;2-A

Reference yield:

: 220116-88-1
(2R,6S)-2-tert-Butyl-6-isobutyl-4-methoxy-5,6-dihydro-2H-pyrimidine-1-carboxylic acid benzyl ester

: (2S,3S)-3-Amino-2-benzyl-5-methyl-hexanoic acid methyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 78 percent / LDA / tetrahydrofuran / 6 h / -78 - -30 °C

2: H₂ / 10percent Pd-C / methanol / 12 h / Ambient temperature

3: aq 0.1 N CF₃COOH / tetrahydrofuran / 96 h / 4 °C

With hydrogen; trifluoroacetic acid; lithium diisopropyl amide; palladium on activated charcoal; In tetrahydrofuran; methanol;
DOI:10.1002/(SICI)1099-0690(199901)1999:1<335::AID-EJOC335>3.0.CO;2-A