(Z)-7-((1R,2R,3R,5S)-2-{(E)-(R)-4-[3-(tert-Butyl-dimethyl-silanyloxy)-5-(trityl-amino)-phenoxy]-3-hydroxy-but-1-enyl}-3,5-dihydroxy-cyclopentyl)-hept-5-enoic acid

Base Information

Chemical Name:(Z)-7-((1R,2R,3R,5S)-2-{(E)-(R)-4-[3-(tert-Butyl-dimethyl-silanyloxy)-5-(trityl-amino)-phenoxy]-3-hydroxy-but-1-enyl}-3,5-dihydroxy-cyclopentyl)-hept-5-enoic acid
CAS No.:117625-65-7
Molecular Formula:C₄₇H₅₉NO₇Si
Molecular Weight:778.073
Hs Code.:

(Z)-7-((1R,2R,3R,5S)-2-{(E)-(R)-4-[3-(tert-Butyl-dimethyl-silanyloxy)-5-(trityl-amino)-phenoxy]-3-hydroxy-but-1-enyl}-3,5-dihydroxy-cyclopentyl)-hept-5-enoic acid

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Chemical Property of (Z)-7-((1R,2R,3R,5S)-2-{(E)-(R)-4-[3-(tert-Butyl-dimethyl-silanyloxy)-5-(trityl-amino)-phenoxy]-3-hydroxy-but-1-enyl}-3,5-dihydroxy-cyclopentyl)-hept-5-enoic acid

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Technology Process of (Z)-7-((1R,2R,3R,5S)-2-{(E)-(R)-4-[3-(tert-Butyl-dimethyl-silanyloxy)-5-(trityl-amino)-phenoxy]-3-hydroxy-but-1-enyl}-3,5-dihydroxy-cyclopentyl)-hept-5-enoic acid

There total 12 articles about (Z)-7-((1R,2R,3R,5S)-2-{(E)-(R)-4-[3-(tert-Butyl-dimethyl-silanyloxy)-5-(trityl-amino)-phenoxy]-3-hydroxy-but-1-enyl}-3,5-dihydroxy-cyclopentyl)-hept-5-enoic acid 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:

: 51642-28-5
5-azidobenzene-1,3-diol

: 117625-65-7
(Z)-7-((1R,2R,3R,5S)-2-{(E)-(R)-4-[3-(tert-Butyl-dimethyl-silanyloxy)-5-(trityl-amino)-phenoxy]-3-hydroxy-but-1-enyl}-3,5-dihydroxy-cyclopentyl)-hept-5-enoic acid

Guidance literature:: Multi-step reaction with 10 steps

1: Et₃N

2: imidazole

3: H₂ / Pd-C

4: Py

5: 1) n-BuLi

6: 1) NaH

7: NaBH₄, CeCl₃

8: K₂CO₃, MeOH

9: DIBAL

With pyridine; 1H-imidazole; methanol; sodium tetrahydroborate; n-butyllithium; cerium(III) chloride; hydrogen; sodium hydride; diisobutylaluminium hydride; potassium carbonate; triethylamine; palladium on activated charcoal;
DOI:10.1021/jm00121a046

Reference yield:

: 18162-48-6
tert-butyldimethylsilyl chloride

: 117625-65-7
(Z)-7-((1R,2R,3R,5S)-2-{(E)-(R)-4-[3-(tert-Butyl-dimethyl-silanyloxy)-5-(trityl-amino)-phenoxy]-3-hydroxy-but-1-enyl}-3,5-dihydroxy-cyclopentyl)-hept-5-enoic acid

Guidance literature:: Multi-step reaction with 9 steps

1: imidazole

2: H₂ / Pd-C

3: Py

4: 1) n-BuLi

5: 1) NaH

6: NaBH₄, CeCl₃

7: K₂CO₃, MeOH

8: DIBAL

With pyridine; 1H-imidazole; methanol; sodium tetrahydroborate; n-butyllithium; cerium(III) chloride; hydrogen; sodium hydride; diisobutylaluminium hydride; potassium carbonate; palladium on activated charcoal;
DOI:10.1021/jm00121a046

Reference yield:

: 114970-03-5
methyl (3-azido-5-hydroxyphenoxy)acetate

: 117625-65-7
(Z)-7-((1R,2R,3R,5S)-2-{(E)-(R)-4-[3-(tert-Butyl-dimethyl-silanyloxy)-5-(trityl-amino)-phenoxy]-3-hydroxy-but-1-enyl}-3,5-dihydroxy-cyclopentyl)-hept-5-enoic acid

Guidance literature:: Multi-step reaction with 9 steps

1: imidazole

2: H₂ / Pd-C

3: Py

4: 1) n-BuLi

5: 1) NaH

6: NaBH₄, CeCl₃

7: K₂CO₃, MeOH

8: DIBAL

With pyridine; 1H-imidazole; methanol; sodium tetrahydroborate; n-butyllithium; cerium(III) chloride; hydrogen; sodium hydride; diisobutylaluminium hydride; potassium carbonate; palladium on activated charcoal;
DOI:10.1021/jm00121a046