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(R,R)-(6'-iodo-N-carbobenzyloxytryptophyl)-3',5'-dichloro-4'-hydroxyphenylglycine tert-butyl ester

Base Information
  • Chemical Name:(R,R)-(6'-iodo-N-carbobenzyloxytryptophyl)-3',5'-dichloro-4'-hydroxyphenylglycine tert-butyl ester
  • CAS No.:872876-83-0
  • Molecular Formula:C31H30Cl2IN3O6
  • Molecular Weight:738.406
  • Hs Code.:
(R,R)-(6'-iodo-N-carbobenzyloxytryptophyl)-3',5'-dichloro-4'-hydroxyphenylglycine tert-butyl ester

Synonyms:(R,R)-(6'-iodo-N-carbobenzyloxytryptophyl)-3',5'-dichloro-4'-hydroxyphenylglycine tert-butyl ester

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Chemical Property of (R,R)-(6'-iodo-N-carbobenzyloxytryptophyl)-3',5'-dichloro-4'-hydroxyphenylglycine tert-butyl ester
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Technology Process of (R,R)-(6'-iodo-N-carbobenzyloxytryptophyl)-3',5'-dichloro-4'-hydroxyphenylglycine tert-butyl ester

There total 11 articles about (R,R)-(6'-iodo-N-carbobenzyloxytryptophyl)-3',5'-dichloro-4'-hydroxyphenylglycine tert-butyl 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:
Guidance literature:
With pentafluorophenyl diphenyl-phosphinate; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; at 20 ℃; for 24h;
DOI:10.1248/cpb.53.1277
Guidance literature:
Multi-step reaction with 9 steps
1: 96 percent / pyridine / 1.4 h / 20 °C
2: 100 percent / H2 / Pd/C / methanol / 1.4 h / 20 °C
3: 62 percent / aq. NaNO2; AcOH; KI / 24 h / 0 °C
4: 71 percent / aq. NaOH / methanol / 4.5 h / 75 °C
5: 98 percent / salcomine; O2 / methanol / 3.5 h / 20 °C
6: 89 percent / AcOH / 2 h / 75 °C
7: 48.3 percent / D-aminocyclase; aq. phosphate buffer; CoCl2 / 47 h / 37 °C / pH 7.4
8: 100 percent / aq. Na2CO3 / diethyl ether / 3 h / 0 °C
9: 64 percent / i-Pr2NEt; FDPP / tetrahydrofuran / 24 h / 20 °C
With pyridine; sodium hydroxide; phosphate buffer; D-aminocyclase; salcomine; pentafluorophenyl diphenyl-phosphinate; hydrogen; oxygen; sodium carbonate; acetic acid; N-ethyl-N,N-diisopropylamine; potassium iodide; sodium nitrite; palladium on activated charcoal; In tetrahydrofuran; methanol; diethyl ether;
DOI:10.1248/cpb.53.1277
Guidance literature:
Multi-step reaction with 8 steps
1: 100 percent / H2 / Pd/C / methanol / 1.4 h / 20 °C
2: 62 percent / aq. NaNO2; AcOH; KI / 24 h / 0 °C
3: 71 percent / aq. NaOH / methanol / 4.5 h / 75 °C
4: 98 percent / salcomine; O2 / methanol / 3.5 h / 20 °C
5: 89 percent / AcOH / 2 h / 75 °C
6: 48.3 percent / D-aminocyclase; aq. phosphate buffer; CoCl2 / 47 h / 37 °C / pH 7.4
7: 100 percent / aq. Na2CO3 / diethyl ether / 3 h / 0 °C
8: 64 percent / i-Pr2NEt; FDPP / tetrahydrofuran / 24 h / 20 °C
With sodium hydroxide; phosphate buffer; D-aminocyclase; salcomine; pentafluorophenyl diphenyl-phosphinate; hydrogen; oxygen; sodium carbonate; acetic acid; N-ethyl-N,N-diisopropylamine; potassium iodide; sodium nitrite; palladium on activated charcoal; In tetrahydrofuran; methanol; diethyl ether;
DOI:10.1248/cpb.53.1277
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