C₄₄H₇₀N₁₂O₁₃

Base Information Edit

Chemical Name:C₄₄H₇₀N₁₂O₁₃
CAS No.:1012050-70-2
Molecular Formula:C₄₄H₇₀N₁₂O₁₃
Molecular Weight:975.112
Hs Code.:
Mol file:1012050-70-2.mol

C<sub>44</sub>H<sub>70</sub>N<sub>12</sub>O<sub>13</sub>

Synonyms:C₄₄H₇₀N₁₂O₁₃

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Chemical Property of C₄₄H₇₀N₁₂O₁₃ Edit

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Technology Process of C₄₄H₇₀N₁₂O₁₃

There total 4 articles about C₄₄H₇₀N₁₂O₁₃ 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: 46.0%

: 756525-91-4
3-[2-[2-[2-[2-(tert-butoxycarbonylamino)ethoxy]ethoxy]ethoxy]ethoxy]propanoic acid

: 1012048-05-3
RGD-C₂

: 1012050-70-2
C₄₄H₇₀N₁₂O₁₃

Guidance literature:: 3-[2-[2-[2-[2-(tert-butoxycarbonylamino)ethoxy]ethoxy]ethoxy]ethoxy]propanoic acid; With 1-hydroxy-pyrrolidine-2,5-dione; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In N,N-dimethyl-formamide; at 20 ℃; for 1h;

RGD-C₂; With N-ethyl-N,N-diisopropylamine; In N,N-dimethyl-formamide; for 6h;

Reference yield:

: 571148-21-5
2-[2-(2-amino-5-{3-[(2,2,4,6,7-pentamethyl-2,3-dihydro-1-benzofuran-5-yl) sulfonyl]carbamimidamido}pentanamido)acetamido]-4-(tert-butoxy)-4-oxobutanoic acid

: 1012050-70-2
C₄₄H₇₀N₁₂O₁₃

Guidance literature:: Multi-step reaction with 5 steps

1.1: benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / dichloromethane / 2 h / 20 °C

1.2: 12 h

2.1: copper(II) sulfate; sodium L-ascorbate / tetrahydrofuran; water; tert-butyl alcohol / 1 h / 20 °C

3.1: benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / dichloromethane / 12 h / 20 °C

4.1: chlorotriisopropylsilane; water; trifluoroacetic acid / 2.5 h / 20 °C

5.1: 1-hydroxy-pyrrolidine-2,5-dione; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / N,N-dimethyl-formamide / 1 h / 20 °C

5.2: 6 h

With 1-hydroxy-pyrrolidine-2,5-dione; chlorotriisopropylsilane; water; benzotriazol-1-ol; copper(II) sulfate; sodium L-ascorbate; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; trifluoroacetic acid; In tetrahydrofuran; dichloromethane; water; N,N-dimethyl-formamide; tert-butyl alcohol;

Reference yield:

: 1012049-17-0
C₄₀H₆₄N₁₀O₁₂S

: 1012050-70-2
C₄₄H₇₀N₁₂O₁₃

Guidance literature:: Multi-step reaction with 4 steps

1.1: copper(II) sulfate; sodium L-ascorbate / tetrahydrofuran; water; tert-butyl alcohol / 1 h / 20 °C

2.1: benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / dichloromethane / 12 h / 20 °C

3.1: chlorotriisopropylsilane; water; trifluoroacetic acid / 2.5 h / 20 °C

4.1: 1-hydroxy-pyrrolidine-2,5-dione; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / N,N-dimethyl-formamide / 1 h / 20 °C

4.2: 6 h

With 1-hydroxy-pyrrolidine-2,5-dione; chlorotriisopropylsilane; water; benzotriazol-1-ol; copper(II) sulfate; sodium L-ascorbate; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; trifluoroacetic acid; In tetrahydrofuran; dichloromethane; water; N,N-dimethyl-formamide; tert-butyl alcohol;