(4-{6-[(9H-fluoren-2-yl)-(toluene-4-sulfonyl)-amino]-hexylamino}-butyl)-carbamic acid benzyl ester

Base Information

• Chemical Name: (4-{6-[(9H-fluoren-2-yl)-(toluene-4-sulfonyl)-amino]-hexylamino}-butyl)-carbamic acid benzyl ester
• CAS No.: 261949-74-0
• Molecular Formula: C₃₈H₄₅N₃O₄S
• Molecular Weight: 639.859

Synonyms:(4-{6-[(9H-fluoren-2-yl)-(toluene-4-sulfonyl)-amino]-hexylamino}-butyl)-carbamic acid benzyl ester

Chemical Property of (4-{6-[(9H-fluoren-2-yl)-(toluene-4-sulfonyl)-amino]-hexylamino}-butyl)-carbamic acid benzyl ester

Chemical Property:

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Technology Process of (4-{6-[(9H-fluoren-2-yl)-(toluene-4-sulfonyl)-amino]-hexylamino}-butyl)-carbamic acid benzyl ester

There total 9 articles about (4-{6-[(9H-fluoren-2-yl)-(toluene-4-sulfonyl)-amino]-hexylamino}-butyl)-carbamic acid benzyl 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:

1,6-hexanediol (629-11-8) → (4-{6-[(9H-fluoren-2-yl)-(toluene-4-sulfonyl)-amino]-hexylamino}-butyl)-carbamic acid benzyl ester (261949-74-0)

Guidance literature:

Multi-step reaction with 9 steps

1: NaH / dimethylformamide / 6 h

2: PCC / CH₂Cl₂

3: Et₃N / CH₂Cl₂ / 12 h

4: NaBH₄ / methanol / 12 h

5: 93 percent / Et₃N / CH₂Cl₂ / 12 h

6: 92 percent / H₂ / Pd/C / ethanol / 12 h

7: 95 percent / PCC / CH₂Cl₂ / 6 h

8: Et₃N / CH₂Cl₂ / 12 h

9: NaBH₄ / methanol / 12 h

With sodium tetrahydroborate; hydrogen; sodium hydride; triethylamine; pyridinium chlorochromate; palladium on activated charcoal; In methanol; ethanol; dichloromethane; N,N-dimethyl-formamide; 1: Substitution / 2: Oxidation / 3: Condensation / 4: Reduction / 5: Tosylation / 6: Hydrogenolysis / 7: Oxidation / 8: Condensation / 9: Reduction;

DOI:10.1016/S0040-4039(99)02094-8

Reference yield:

6-benzyloxyhexan-1-ol (71126-73-3) → (4-{6-[(9H-fluoren-2-yl)-(toluene-4-sulfonyl)-amino]-hexylamino}-butyl)-carbamic acid benzyl ester (261949-74-0)

Guidance literature:

Multi-step reaction with 8 steps

1: PCC / CH₂Cl₂

2: Et₃N / CH₂Cl₂ / 12 h

3: NaBH₄ / methanol / 12 h

4: 93 percent / Et₃N / CH₂Cl₂ / 12 h

5: 92 percent / H₂ / Pd/C / ethanol / 12 h

6: 95 percent / PCC / CH₂Cl₂ / 6 h

7: Et₃N / CH₂Cl₂ / 12 h

8: NaBH₄ / methanol / 12 h

With sodium tetrahydroborate; hydrogen; triethylamine; pyridinium chlorochromate; palladium on activated charcoal; In methanol; ethanol; dichloromethane; 1: Oxidation / 2: Condensation / 3: Reduction / 4: Tosylation / 5: Hydrogenolysis / 6: Oxidation / 7: Condensation / 8: Reduction;

DOI:10.1016/S0040-4039(99)02094-8

Reference yield:

6-benzyloxy-1-hexanal (101492-91-5) → (4-{6-[(9H-fluoren-2-yl)-(toluene-4-sulfonyl)-amino]-hexylamino}-butyl)-carbamic acid benzyl ester (261949-74-0)

Guidance literature:

Multi-step reaction with 7 steps

1: Et₃N / CH₂Cl₂ / 12 h

2: NaBH₄ / methanol / 12 h

3: 93 percent / Et₃N / CH₂Cl₂ / 12 h

4: 92 percent / H₂ / Pd/C / ethanol / 12 h

5: 95 percent / PCC / CH₂Cl₂ / 6 h

6: Et₃N / CH₂Cl₂ / 12 h

7: NaBH₄ / methanol / 12 h

With sodium tetrahydroborate; hydrogen; triethylamine; pyridinium chlorochromate; palladium on activated charcoal; In methanol; ethanol; dichloromethane; 1: Condensation / 2: Reduction / 3: Tosylation / 4: Hydrogenolysis / 5: Oxidation / 6: Condensation / 7: Reduction;

DOI:10.1016/S0040-4039(99)02094-8

upstream raw materials:

1,6-hexanediol

6-benzyloxyhexan-1-ol

6-benzyloxy-1-hexanal

(6-benzyloxy-hexyl)-(9H-fluoren-2-yl)-amine

Downstream raw materials:

{4-[6-(9H-fluoren-2-ylamino)-hexylamino]-butyl}-carbamic acid benzyl ester

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