2-Phenyl-N-[6-(2-phenyl-butyrylamino)-4-undec-10-enyloxy-pyridin-2-yl]-butyramide

Base Information

• Chemical Name: 2-Phenyl-N-[6-(2-phenyl-butyrylamino)-4-undec-10-enyloxy-pyridin-2-yl]-butyramide
• CAS No.: 101631-03-2
• Molecular Formula: C₃₆H₄₇N₃O₃
• Molecular Weight: 569.787
• Mol file: 101631-03-2.mol

Synonyms:2-Phenyl-N-[6-(2-phenyl-butyrylamino)-4-undec-10-enyloxy-pyridin-2-yl]-butyramide

Chemical Property of 2-Phenyl-N-[6-(2-phenyl-butyrylamino)-4-undec-10-enyloxy-pyridin-2-yl]-butyramide

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of 2-Phenyl-N-[6-(2-phenyl-butyrylamino)-4-undec-10-enyloxy-pyridin-2-yl]-butyramide

There total 7 articles about 2-Phenyl-N-[6-(2-phenyl-butyrylamino)-4-undec-10-enyloxy-pyridin-2-yl]-butyramide 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: 25.0%

(S)-(+)-2-phenylbutyric acid chloride (40473-35-6) + 2,6-diamino-4-(10-undecenyloxy)pyridine (101631-02-1) → <4-(undecyloxy)-2,6-pyridinediyl>bis<(S)-2-phenylbutanamide> + 2-Phenyl-N-[6-(2-phenyl-butyrylamino)-4-undec-10-enyloxy-pyridin-2-yl]-butyramide (101631-03-2) + N,N'-<4-(10-undecenyloxy)-2,6-pyridinediyl>bis<(S)-2-phenylbutanamide> (101693-76-9)

Guidance literature:

With 4-methyl-morpholine; In chloroform; at -20 - -15 ℃;

DOI:10.1021/ja00272a027

Reference yield:

1-undecen-11-ylbromide (7766-50-9) → 2-Phenyl-N-[6-(2-phenyl-butyrylamino)-4-undec-10-enyloxy-pyridin-2-yl]-butyramide (101631-03-2)

Guidance literature:

Multi-step reaction with 6 steps

1: 1.) Na / 2.) 18-crown-6 / 1.) butanol; 2.) toluene, reflux, overnight

2: 65 percent / H₂NNH₂ / by Markees et al.

3: 9percent HCl, NaNO₂ / H₂O / 2 h / 10 - 15 °C

4: 5 h / Heating

5: 85 percent / KOH / ethanol / 3 h / Heating

6: N-methylmorpholine / CHCl₃ / -20 - -15 °C

With 4-methyl-morpholine; hydrogenchloride; potassium hydroxide; sodium; hydrazine; sodium nitrite; 18-crown-6 ether; In ethanol; chloroform; water;

DOI:10.1021/ja00272a027

Reference yield:

(S)-2-phenylbutyric acid (4286-15-1) → 2-Phenyl-N-[6-(2-phenyl-butyrylamino)-4-undec-10-enyloxy-pyridin-2-yl]-butyramide (101631-03-2)

Guidance literature:

Multi-step reaction with 2 steps

1: 80 percent / SOCl₂ / CH₂Cl₂ / 4 h / Heating

2: N-methylmorpholine / CHCl₃ / -20 - -15 °C

With 4-methyl-morpholine; thionyl chloride; In dichloromethane; chloroform;

DOI:10.1021/ja00272a027

upstream raw materials:

(S)-(+)-2-phenylbutyric acid chloride

2,6-diamino-4-(10-undecenyloxy)pyridine

1-undecen-11-ylbromide

(S)-2-phenylbutyric acid