Technology Process of 1,2-Pyrrolidinedicarboxylic acid,
5-[(2Z)-4-methoxy-4-oxo-2-phenyl-3-[[(phenylmethoxy)carbonyl]amino]-
2-butenyl]-, 1-(1,1-dimethylethyl) 2-methyl ester, (2S,5R)-
There total 5 articles about 1,2-Pyrrolidinedicarboxylic acid,
5-[(2Z)-4-methoxy-4-oxo-2-phenyl-3-[[(phenylmethoxy)carbonyl]amino]-
2-butenyl]-, 1-(1,1-dimethylethyl) 2-methyl ester, (2S,5R)- 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:
- Guidance literature:
-
With
palladium diacetate; sodium carbonate; tris-(o-tolyl)phosphine;
In
1,2-dimethoxyethane; water;
at 80 ℃;
DOI:10.1021/ol020160a
- Guidance literature:
-
Multi-step reaction with 7 steps
1.1: LiBEt3H / tetrahydrofuran / 0.67 h / -78 °C
2.1: p-TsOH / 20 °C
3.1: 1.78 g / BF3*Et2O / diethyl ether / 0.25 h / -40 °C
4.1: OsO4; NaIO4 / tetrahydrofuran; H2O / 4 h / 20 °C
5.1: 1.95 g / DBU / CH2Cl2 / 8 h / 20 °C
6.1: NBS / CHCl3 / 1.33 h / 20 °C
6.2: 53 percent / DABCO / CHCl3 / 24 h / 20 °C
7.1: 76 percent / Pd(OAc)2; P(o-tolyl)3; Na2CO3 / 1,2-dimethoxy-ethane; H2O / 80 °C
With
palladium diacetate; sodium periodate; N-Bromosuccinimide; osmium(VIII) oxide; boron trifluoride diethyl etherate; lithium triethylborohydride; sodium carbonate; toluene-4-sulfonic acid; 1,8-diazabicyclo[5.4.0]undec-7-ene; tris-(o-tolyl)phosphine;
In
tetrahydrofuran; 1,2-dimethoxyethane; diethyl ether; dichloromethane; chloroform; water;
5.1: Horner-Emmons olefination / 7.1: Suzuki cross-coupling;
DOI:10.1021/ol020160a
- Guidance literature:
-
Multi-step reaction with 6 steps
1.1: p-TsOH / 20 °C
2.1: 1.78 g / BF3*Et2O / diethyl ether / 0.25 h / -40 °C
3.1: OsO4; NaIO4 / tetrahydrofuran; H2O / 4 h / 20 °C
4.1: 1.95 g / DBU / CH2Cl2 / 8 h / 20 °C
5.1: NBS / CHCl3 / 1.33 h / 20 °C
5.2: 53 percent / DABCO / CHCl3 / 24 h / 20 °C
6.1: 76 percent / Pd(OAc)2; P(o-tolyl)3; Na2CO3 / 1,2-dimethoxy-ethane; H2O / 80 °C
With
palladium diacetate; sodium periodate; N-Bromosuccinimide; osmium(VIII) oxide; boron trifluoride diethyl etherate; sodium carbonate; toluene-4-sulfonic acid; 1,8-diazabicyclo[5.4.0]undec-7-ene; tris-(o-tolyl)phosphine;
In
tetrahydrofuran; 1,2-dimethoxyethane; diethyl ether; dichloromethane; chloroform; water;
4.1: Horner-Emmons olefination / 6.1: Suzuki cross-coupling;
DOI:10.1021/ol020160a