C₆₁H₈₀N₆O₁₃

Base Information

Chemical Name:C₆₁H₈₀N₆O₁₃
CAS No.:405555-29-5
Molecular Formula:C₆₁H₈₀N₆O₁₃
Molecular Weight:1105.34
Hs Code.:

C<sub>61</sub>H<sub>80</sub>N<sub>6</sub>O<sub>13</sub>

Synonyms:C₆₁H₈₀N₆O₁₃

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Chemical Property of C₆₁H₈₀N₆O₁₃

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Technology Process of C₆₁H₈₀N₆O₁₃

There total 11 articles about C₆₁H₈₀N₆O₁₃ 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: 78.0%

: 405928-07-6
C₆₁H₈₂N₆O₁₃

: 405555-29-5
C₆₁H₈₀N₆O₁₃

Guidance literature:: With aluminum oxide; pyridinium chlorochromate; In dichloromethane; at 20 ℃; for 5h;
DOI:10.1021/jo0160569

Reference yield:

: 96238-70-9
1-tert-butoxycarbonyl-L-tryptophane methyl ester

: 405555-29-5
C₆₁H₈₀N₆O₁₃

Guidance literature:: Multi-step reaction with 7 steps

1: 84 percent / HBTU; DIEA / dimethylformamide / 2.5 h / 20 °C

2: 83 percent / hydrogen / 10percent Pd/C / methanol / 3 h / 20 °C / 760.05 Torr

3: AcOH; 4 Angstroem molecular sieves / CDCl₃ / 50 °C

4: 0.574 g / NaBH₄ / methanol / 0.5 h / 0 - 20 °C

5: 69 percent / DIEA; HBTU / dimethylformamide / 6 h / 40 °C

6: 79 percent / Zn(BF₄)2 / acetonitrile; H₂O / 7 h / 20 °C

7: 78 percent / pyridinium chlorochromate; Al₂O₃ / CH₂Cl₂ / 5 h / 20 °C

With aluminum oxide; sodium tetrahydroborate; zinc tetrafluoroborate; 4 A molecular sieve; hydrogen; O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate; acetic acid; N-ethyl-N,N-diisopropylamine; pyridinium chlorochromate; 10percent Pd/C; In methanol; chloroform-d1; dichloromethane; water; N,N-dimethyl-formamide; acetonitrile;
DOI:10.1021/jo0160569

Reference yield:

: 143824-78-6,163619-04-3
3-[(S)-2-carboxy-2-(9H-fluoren-9-ylmethoxycarbonylamino)ethyl]indole-1-carboxylic acid tert-butyl ester

: 405555-29-5
C₆₁H₈₀N₆O₁₃

Guidance literature:: Multi-step reaction with 9 steps

1: 83 percent / DMAP; EDC / 1 h / 20 °C

2: 67 percent / piperidine / dimethylformamide / 0.5 h / 20 °C

3: 84 percent / HBTU; DIEA / dimethylformamide / 2.5 h / 20 °C

4: 83 percent / hydrogen / 10percent Pd/C / methanol / 3 h / 20 °C / 760.05 Torr

5: AcOH; 4 Angstroem molecular sieves / CDCl₃ / 50 °C

6: 0.574 g / NaBH₄ / methanol / 0.5 h / 0 - 20 °C

7: 69 percent / DIEA; HBTU / dimethylformamide / 6 h / 40 °C

8: 79 percent / Zn(BF₄)2 / acetonitrile; H₂O / 7 h / 20 °C

9: 78 percent / pyridinium chlorochromate; Al₂O₃ / CH₂Cl₂ / 5 h / 20 °C

With piperidine; dmap; aluminum oxide; sodium tetrahydroborate; zinc tetrafluoroborate; 4 A molecular sieve; hydrogen; O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate; acetic acid; N-(3-dimethylaminopropyl)-N-ethylcarbodiimide; N-ethyl-N,N-diisopropylamine; pyridinium chlorochromate; 10percent Pd/C; In methanol; chloroform-d1; dichloromethane; water; N,N-dimethyl-formamide; acetonitrile;
DOI:10.1021/jo0160569