(3S,5S)-5-Benzyloxy-tetrahydro-pyridazine-1,3-dicarboxylic acid 1-benzyl ester 3-methyl ester

Base Information

Chemical Name:(3S,5S)-5-Benzyloxy-tetrahydro-pyridazine-1,3-dicarboxylic acid 1-benzyl ester 3-methyl ester
CAS No.:214354-16-2
Molecular Formula:C₂₁H₂₄N₂O₅
Molecular Weight:384.432
Hs Code.:

Synonyms:(3S,5S)-5-Benzyloxy-tetrahydro-pyridazine-1,3-dicarboxylic acid 1-benzyl ester 3-methyl ester

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Chemical Property of (3S,5S)-5-Benzyloxy-tetrahydro-pyridazine-1,3-dicarboxylic acid 1-benzyl ester 3-methyl ester

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Technology Process of (3S,5S)-5-Benzyloxy-tetrahydro-pyridazine-1,3-dicarboxylic acid 1-benzyl ester 3-methyl ester

There total 3 articles about (3S,5S)-5-Benzyloxy-tetrahydro-pyridazine-1,3-dicarboxylic acid 1-benzyl ester 3-methyl 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:

: 501-53-1,94274-21-2
benzyl chloroformate

: (3S,5S)-5-Benzyloxy-hexahydro-pyridazine-3-carboxylic acid methyl ester

: 214354-16-2
(3S,5S)-5-Benzyloxy-tetrahydro-pyridazine-1,3-dicarboxylic acid 1-benzyl ester 3-methyl ester

Guidance literature:: With sodium hydrogencarbonate; In dichloromethane; at 0 ℃; for 0.833333h; Yield given;
DOI:10.1016/S0040-4039(98)01533-0

Reference yield:

: 214354-11-7
(3S,5S)-5-Benzyloxy-tetrahydro-pyridazine-1,2,3-tricarboxylic acid 1,2-di-tert-butyl ester 3-methyl ester

: 214354-16-2
(3S,5S)-5-Benzyloxy-tetrahydro-pyridazine-1,3-dicarboxylic acid 1-benzyl ester 3-methyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: trifluoroacetic acid / CH₂Cl₂ / 2.5 h / Ambient temperature

2: aq. NaHCO₃ / CH₂Cl₂ / 0.83 h / 0 °C

With sodium hydrogencarbonate; trifluoroacetic acid; In dichloromethane;
DOI:10.1016/S0040-4039(98)01533-0

Reference yield:

: 214354-03-7
(3S,5S)-3-((S)-4-Benzyl-2-oxo-oxazolidine-3-carbonyl)-5-benzyloxy-tetrahydro-pyridazine-1,2-dicarboxylic acid di-tert-butyl ester

: 214354-16-2
(3S,5S)-5-Benzyloxy-tetrahydro-pyridazine-1,3-dicarboxylic acid 1-benzyl ester 3-methyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 93 percent / NaOMe / CH₂Cl₂ / 0.25 h / -30 °C

2: trifluoroacetic acid / CH₂Cl₂ / 2.5 h / Ambient temperature

3: aq. NaHCO₃ / CH₂Cl₂ / 0.83 h / 0 °C

With sodium methylate; sodium hydrogencarbonate; trifluoroacetic acid; In dichloromethane;
DOI:10.1016/S0040-4039(98)01533-0