<γR(1'S,2'R),(1R)>-acide-δ-<1-(Nb-benzyl-tetrahydro-β-carboline)>-γ-<1'-(3'-O-p-nitrobenzoyl-1',2',3'-trihydroxypropyl)>-butyrique-1',α-γ-lactone

Base Information

Chemical Name:<γR(1'S,2'R),(1R)>-acide-δ-<1-(Nb-benzyl-tetrahydro-β-carboline)>-γ-<1'-(3'-O-p-nitrobenzoyl-1',2',3'-trihydroxypropyl)>-butyrique-1',α-γ-lactone
CAS No.:144808-37-7
Molecular Formula:C₃₂H₃₁N₃O₇
Molecular Weight:569.614
Hs Code.:

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Chemical Property of <γR(1'S,2'R),(1R)>-acide-δ-<1-(Nb-benzyl-tetrahydro-β-carboline)>-γ-<1'-(3'-O-p-nitrobenzoyl-1',2',3'-trihydroxypropyl)>-butyrique-1',α-γ-lactone

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Technology Process of <γR(1'S,2'R),(1R)>-acide-δ-<1-(Nb-benzyl-tetrahydro-β-carboline)>-γ-<1'-(3'-O-p-nitrobenzoyl-1',2',3'-trihydroxypropyl)>-butyrique-1',α-γ-lactone

There total 10 articles about <γR(1'S,2'R),(1R)>-acide-δ-<1-(Nb-benzyl-tetrahydro-β-carboline)>-γ-<1'-(3'-O-p-nitrobenzoyl-1',2',3'-trihydroxypropyl)>-butyrique-1',α-γ-lactone 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: 38.0%

: 15741-79-4
N-benzyl tryptamine

: 213969-31-4
6-O-p-nitrobenzoyl-3-C-(carboxymethylene)-2,3-didesoxy-α-β-D-ribo-hexapyranose-2,4-γ-lactone

: 144808-37-7,144808-40-2
<γR(1'S,2'R),(1S)>-acide-δ-<1-(Nb-benzyl-tetrahydro-β-carboline)>-γ-<1'-(3'-O-p-nitrobenzoyl-1',2',3'-trihydroxypropyl)>-butyrique-1',α-γ-lactone

: 144808-37-7,144808-40-2
<γR(1'S,2'R),(1R)>-acide-δ-<1-(Nb-benzyl-tetrahydro-β-carboline)>-γ-<1'-(3'-O-p-nitrobenzoyl-1',2',3'-trihydroxypropyl)>-butyrique-1',α-γ-lactone

Guidance literature:: With acetic acid; In benzene; for 3h; Heating;
DOI:10.1016/S0040-4020(01)80014-4

Reference yield: 38.0%

: 15741-79-4
N-benzyl tryptamine

: 213969-31-4
6-O-p-nitrobenzoyl-3-C-(carboxymethylene)-2,3-didesoxy-α-β-D-ribo-hexapyranose-2,4-γ-lactone

: 144808-37-7,144808-40-2
<γR(1'S,2'R),(1S)>-acide-δ-<1-(Nb-benzyl-tetrahydro-β-carboline)>-γ-<1'-(3'-O-p-nitrobenzoyl-1',2',3'-trihydroxypropyl)>-butyrique-1',α-γ-lactone

: 144808-37-7,144808-40-2
<γR(1'S,2'R),(1R)>-acide-δ-<1-(Nb-benzyl-tetrahydro-β-carboline)>-γ-<1'-(3'-O-p-nitrobenzoyl-1',2',3'-trihydroxypropyl)>-butyrique-1',α-γ-lactone

Guidance literature:: With acetic acid; In benzene; for 3h; Heating;
DOI:10.1016/S0040-4020(01)80014-4

Reference yield:

: 88901-92-2
methyl 4,6-O-benzylidene-3-C-(carbomethoxy-methylene)-2,3-didesoxy-α-D-ribo-hexapyranoside

: 144808-37-7,144808-40-2
<γR(1'S,2'R),(1S)>-acide-δ-<1-(Nb-benzyl-tetrahydro-β-carboline)>-γ-<1'-(3'-O-p-nitrobenzoyl-1',2',3'-trihydroxypropyl)>-butyrique-1',α-γ-lactone

Guidance literature:: Multi-step reaction with 4 steps

1: 80 percent / hydrogen / 10percent Pd-C / methanol / 12 h

2: 80 percent / pyridine / 20 deg C, 24 h, then 70 deg C, 1 h

3: 87 percent / acetic acid, water / 12 h / Heating

4: 37 percent / acetic acid / benzene / 3 h / Heating

With pyridine; water; hydrogen; acetic acid; palladium on activated charcoal; In methanol; benzene;
DOI:10.1016/S0040-4020(01)80014-4