phenylmethyl -<2-<<3-(1H-indol-3-yl)-2-<(4-oxo-3-oxa-1-azaspiro<4.5>dec-1-en-2-yl)amino>-1-oxopropyl>amino>-1-phenylethyl>carbamate

Base Information

Chemical Name:phenylmethyl -<2-<<3-(1H-indol-3-yl)-2-<(4-oxo-3-oxa-1-azaspiro<4.5>dec-1-en-2-yl)amino>-1-oxopropyl>amino>-1-phenylethyl>carbamate
CAS No.:144876-79-9
Molecular Formula:C₃₅H₃₇N₅O₅
Molecular Weight:607.709
Hs Code.:

phenylmethyl <R-(R*,R*)>-<2-<<3-(1H-indol-3-yl)-2-<(4-oxo-3-oxa-1-azaspiro<4.5>dec-1-en-2-yl)amino>-1-oxopropyl>amino>-1-phenylethyl>carbamate

Synonyms:phenylmethyl -<2-<<3-(1H-indol-3-yl)-2-<(4-oxo-3-oxa-1-azaspiro<4.5>dec-1-en-2-yl)amino>-1-oxopropyl>amino>-1-phenylethyl>carbamate

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Chemical Property of phenylmethyl -<2-<<3-(1H-indol-3-yl)-2-<(4-oxo-3-oxa-1-azaspiro<4.5>dec-1-en-2-yl)amino>-1-oxopropyl>amino>-1-phenylethyl>carbamate

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Technology Process of phenylmethyl -<2-<<3-(1H-indol-3-yl)-2-<(4-oxo-3-oxa-1-azaspiro<4.5>dec-1-en-2-yl)amino>-1-oxopropyl>amino>-1-phenylethyl>carbamate

There total 11 articles about phenylmethyl -<2-<<3-(1H-indol-3-yl)-2-<(4-oxo-3-oxa-1-azaspiro<4.5>dec-1-en-2-yl)amino>-1-oxopropyl>amino>-1-phenylethyl>carbamate 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: 95.0%

: 144876-74-4
phenylmethyl -4-(1H-indol-3-ylmethyl)-2,5-dioxo-8-phenyl-1-<1-<<2-(triemthylsilyl)ethoxy>carbonyl>cyclohexyl>-1,3,6,9-tetraazadecan-10-oate

: 144876-79-9
phenylmethyl -<2-<<3-(1H-indol-3-yl)-2-<(4-oxo-3-oxa-1-azaspiro<4.5>dec-1-en-2-yl)amino>-1-oxopropyl>amino>-1-phenylethyl>carbamate

Guidance literature:: With tetrabutyl ammonium fluoride; In tetrahydrofuran; at 0 ℃;
DOI:10.1016/S0040-4020(01)86596-0

Reference yield: 93.0%

: 144876-71-1
phenylmethyl -4-(1H-indol-3-ylmethyl)-1-<1-(methoxycarbonyl)cyclohexyl>-2,5-dioxo-8-phenyl-1,3,6,9-tetraazadecan-10-oate

: 144876-79-9
phenylmethyl -<2-<<3-(1H-indol-3-yl)-2-<(4-oxo-3-oxa-1-azaspiro<4.5>dec-1-en-2-yl)amino>-1-oxopropyl>amino>-1-phenylethyl>carbamate

Guidance literature:: With lithium hydroxide; In tetrahydrofuran; water; at 25 ℃;
DOI:10.1016/S0040-4020(01)86596-0

Reference yield:

: 17191-43-4
1-{[(benzyloxy)carbonyl]amino}cyclohexanecarboxylic acid

: 144876-79-9
phenylmethyl -<2-<<3-(1H-indol-3-yl)-2-<(4-oxo-3-oxa-1-azaspiro<4.5>dec-1-en-2-yl)amino>-1-oxopropyl>amino>-1-phenylethyl>carbamate

Guidance literature:: Multi-step reaction with 5 steps

1: 68 percent / dicyclohexylcarbodiimide, 4-dimethylaminopyridine / acetonitrile; dimethylformamide / 24 h / Ambient temperature

2: 99 percent / H₂ / 20percent Pd(OH)2/C / propan-2-ol / 17 h / 25 °C / 2327.2 Torr

3: 96 percent / NEt₃ / tetrahydrofuran / 25 °C

4: 81 percent / toluene; tetrahydrofuran / 16 h / 80 - 100 °C

5: 95 percent / Bu₄NF / tetrahydrofuran / 0 °C

With dmap; tetrabutyl ammonium fluoride; hydrogen; triethylamine; dicyclohexyl-carbodiimide; palladium dihydroxide; In tetrahydrofuran; N,N-dimethyl-formamide; isopropyl alcohol; toluene; acetonitrile;
DOI:10.1016/S0040-4020(01)86596-0