<3aS-(3aα,4Z,6aα)>-5-imidazol-4-ylidene>pentanoic acid methyl ester

Base Information

Chemical Name:<3aS-(3aα,4Z,6aα)>-5-imidazol-4-ylidene>pentanoic acid methyl ester
CAS No.:151526-80-6
Molecular Formula:C₁₈H₂₂N₂O₃S
Molecular Weight:346.45
Hs Code.:

<3aS-(3aα,4Z,6aα)>-5-<Hexahydro-2-oxo-1-(phenylmethyl)-4H-thieno<3,4-d>imidazol-4-ylidene>pentanoic acid methyl ester

Synonyms:<3aS-(3aα,4Z,6aα)>-5-imidazol-4-ylidene>pentanoic acid methyl ester

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Chemical Property of <3aS-(3aα,4Z,6aα)>-5-imidazol-4-ylidene>pentanoic acid methyl ester

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Technology Process of <3aS-(3aα,4Z,6aα)>-5-imidazol-4-ylidene>pentanoic acid methyl ester

There total 13 articles about <3aS-(3aα,4Z,6aα)>-5-imidazol-4-ylidene>pentanoic acid 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: 32.0%

: 151415-06-4
Δ^2,3,N-(Phenylmethyl)-2-(carbomethoxybutyl)dihydrothiophene-4(S)-carbamoyl azide

: 151415-07-5
<3aS-(3aα,4E,6aα)>-5-imidazol-4-ylidene>pentanoic acid methyl ester

: 151526-80-6
<3aS-(3aα,4Z,6aα)>-5-imidazol-4-ylidene>pentanoic acid methyl ester

Guidance literature:: In dichloromethane; at 150 ℃; for 3h;
DOI:10.1021/jo00107a009

Reference yield:

: 100-52-7
benzaldehyde

: 151526-80-6
<3aS-(3aα,4Z,6aα)>-5-imidazol-4-ylidene>pentanoic acid methyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: citric acid; NaHCO₃; NaBH₃CN / H₂O; tetrahydrofuran / 2.5 h / 5 °C / pH 4

2: 1.4 g / HCl / H₂O; tetrahydrofuran / 21 h / 25 °C

3: 77 percent / NaHCO₃; triethyl phosphite; Pd(OAc)2 / tetrabutylammonium chloride / dimethylformamide; H₂O / 2 h / 100 °C

With hydrogenchloride; palladium diacetate; sodium cyanoborohydride; sodium hydrogencarbonate; citric acid; triethyl phosphite; tetrabutyl-ammonium chloride; In tetrahydrofuran; water; N,N-dimethyl-formamide;
DOI:10.1021/jo025794+

Reference yield:

: 449729-42-4
(S)-7-[(2R,4R)-3-(tert-butoxycarbonyl)-2-phenylthiazolidin-4-yl]-7-hydroxy-6-oxoheptanoic acid methyl ester

: 151526-80-6
<3aS-(3aα,4Z,6aα)>-5-imidazol-4-ylidene>pentanoic acid methyl ester

Guidance literature:: Multi-step reaction with 5 steps

1: 100 percent / triethylamine; 4-(dimethylamino)pyridine / tetrahydrofuran / 2.5 h / 0 °C

2: MeOH; acetyl chloride / toluene / 1 h / 0 °C

3: citric acid; NaHCO₃; NaBH₃CN / H₂O; tetrahydrofuran / 2.5 h / 5 °C / pH 4

4: 1.4 g / HCl / H₂O; tetrahydrofuran / 21 h / 25 °C

5: 77 percent / NaHCO₃; triethyl phosphite; Pd(OAc)2 / tetrabutylammonium chloride / dimethylformamide; H₂O / 2 h / 100 °C

With hydrogenchloride; methanol; dmap; palladium diacetate; sodium cyanoborohydride; sodium hydrogencarbonate; triethylamine; acetyl chloride; citric acid; triethyl phosphite; tetrabutyl-ammonium chloride; In tetrahydrofuran; water; N,N-dimethyl-formamide; toluene;
DOI:10.1021/jo025794+