(1aS,2S,7bS)-2-Ethynyl-7b-((S)-1-hydroxy-ethyl)-1a,7b-dihydro-2H-1-oxa-3-aza-cyclopropa[a]naphthalene-3-carboxylic acid phenyl ester

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Chemical Name:(1aS,2S,7bS)-2-Ethynyl-7b-((S)-1-hydroxy-ethyl)-1a,7b-dihydro-2H-1-oxa-3-aza-cyclopropa[a]naphthalene-3-carboxylic acid phenyl ester
CAS No.:169103-36-0
Molecular Formula:C₂₀H₁₇NO₄
Molecular Weight:335.359
Hs Code.:

Synonyms:(1aS,2S,7bS)-2-Ethynyl-7b-((S)-1-hydroxy-ethyl)-1a,7b-dihydro-2H-1-oxa-3-aza-cyclopropa[a]naphthalene-3-carboxylic acid phenyl ester

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Chemical Property of (1aS,2S,7bS)-2-Ethynyl-7b-((S)-1-hydroxy-ethyl)-1a,7b-dihydro-2H-1-oxa-3-aza-cyclopropa[a]naphthalene-3-carboxylic acid phenyl ester

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Technology Process of (1aS,2S,7bS)-2-Ethynyl-7b-((S)-1-hydroxy-ethyl)-1a,7b-dihydro-2H-1-oxa-3-aza-cyclopropa[a]naphthalene-3-carboxylic acid phenyl ester

There total 6 articles about (1aS,2S,7bS)-2-Ethynyl-7b-((S)-1-hydroxy-ethyl)-1a,7b-dihydro-2H-1-oxa-3-aza-cyclopropa[a]naphthalene-3-carboxylic acid phenyl 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: 89.0%

: 161824-77-7
(R)-2-Ethynyl-4-((S)-1-hydroxy-ethyl)-2H-quinoline-1-carboxylic acid phenyl ester

: 169103-36-0
(1aS,2S,7bS)-2-Ethynyl-7b-((S)-1-hydroxy-ethyl)-1a,7b-dihydro-2H-1-oxa-3-aza-cyclopropa[a]naphthalene-3-carboxylic acid phenyl ester

Guidance literature:: With disodium hydrogenphosphate; 3-chloro-benzenecarboperoxoic acid; In dichloromethane; at 0 ℃; for 2h;
DOI:10.1016/0040-4039(94)80032-4

Reference yield:

: 55908-34-4
1-Quinolin-4-yl-ethanol

: 169103-36-0
(1aS,2S,7bS)-2-Ethynyl-7b-((S)-1-hydroxy-ethyl)-1a,7b-dihydro-2H-1-oxa-3-aza-cyclopropa[a]naphthalene-3-carboxylic acid phenyl ester

Guidance literature:: Multi-step reaction with 6 steps

2: 92 percent / imidazol / dimethylformamide / 19 h / 70 °C

3: 71 percent / CH₂Cl₂ / -78 °C

4: TBAF, MeOH / tetrahydrofuran / 0.42 h / 0 °C

5: TsOH*H₂O, MeOH / 11.5 h / Heating

6: 89 percent / MCPBA, Na₂HPO₄ / CH₂Cl₂ / 2 h / 0 °C

With 1H-imidazole; methanol; disodium hydrogenphosphate; tetrabutyl ammonium fluoride; toluene-4-sulfonic acid; 3-chloro-benzenecarboperoxoic acid; In tetrahydrofuran; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1016/0040-4039(94)80032-4

Reference yield:

: 161907-06-8
(S)-1-(quinolin-4-yl)ethan-1-ol

: 169103-36-0
(1aS,2S,7bS)-2-Ethynyl-7b-((S)-1-hydroxy-ethyl)-1a,7b-dihydro-2H-1-oxa-3-aza-cyclopropa[a]naphthalene-3-carboxylic acid phenyl ester

Guidance literature:: Multi-step reaction with 5 steps

1: 92 percent / imidazol / dimethylformamide / 19 h / 70 °C

2: 71 percent / CH₂Cl₂ / -78 °C

3: TBAF, MeOH / tetrahydrofuran / 0.42 h / 0 °C

4: TsOH*H₂O, MeOH / 11.5 h / Heating

5: 89 percent / MCPBA, Na₂HPO₄ / CH₂Cl₂ / 2 h / 0 °C

With 1H-imidazole; methanol; disodium hydrogenphosphate; tetrabutyl ammonium fluoride; toluene-4-sulfonic acid; 3-chloro-benzenecarboperoxoic acid; In tetrahydrofuran; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1016/0040-4039(94)80032-4