diethyl N-<4-<3-<<2-(pivaloylamino)-6-chloropyrimidin-4-yl>amino>propyl>benzoyl>-L-glutamate

Base Information

Chemical Name:diethyl N-<4-<3-<<2-(pivaloylamino)-6-chloropyrimidin-4-yl>amino>propyl>benzoyl>-L-glutamate
CAS No.:141019-30-9
Molecular Formula:C₂₈H₃₈ClN₅O₆
Molecular Weight:576.093
Hs Code.:

Synonyms:diethyl N-<4-<3-<<2-(pivaloylamino)-6-chloropyrimidin-4-yl>amino>propyl>benzoyl>-L-glutamate

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Chemical Property of diethyl N-<4-<3-<<2-(pivaloylamino)-6-chloropyrimidin-4-yl>amino>propyl>benzoyl>-L-glutamate

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Technology Process of diethyl N-<4-<3-<<2-(pivaloylamino)-6-chloropyrimidin-4-yl>amino>propyl>benzoyl>-L-glutamate

There total 6 articles about diethyl N-<4-<3-<<2-(pivaloylamino)-6-chloropyrimidin-4-yl>amino>propyl>benzoyl>-L-glutamate 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: 82.0%

: 141019-03-6
2-(pivaloylamino)-4,6-dichloropyrimidine

: 141043-86-9
diethyl N-<4-(3-aminopropyl)benzoyl>-L-glutamate

: 141019-30-9
diethyl N-<4-<3-<<2-(pivaloylamino)-6-chloropyrimidin-4-yl>amino>propyl>benzoyl>-L-glutamate

Guidance literature:: With TEA; In tetrahydrofuran; at 25 ℃; for 2h;
DOI:10.1021/jo00037a047

Reference yield:

: 116387-21-4
4-iodobenzoyl-L-glutamic acid diethyl ester

: 141019-30-9
diethyl N-<4-<3-<<2-(pivaloylamino)-6-chloropyrimidin-4-yl>amino>propyl>benzoyl>-L-glutamate

Guidance literature:: Multi-step reaction with 6 steps

1: 74 percent / NaHCO₃, (n-Bu)4NBr, 4-Angstroem sieves / Pd(OAc)2 / 72 h / 25 °C

2: 93 percent / NaBH₄ / methanol / 1 h / 25 °C

3: 94 percent / TEA / tetrahydrofuran / 3 h / 25 °C

4: 93 percent / NaN₃ / dimethylformamide / 18 h / 25 °C

5: 95 percent / water, Ph₃P, / 18 h / 25 °C

6: 82 percent / TEA / tetrahydrofuran / 2 h / 25 °C

With sodium tetrahydroborate; sodium azide; 4 A molecular sieve; TEA; tetrabutylammomium bromide; water; sodium hydrogencarbonate; triphenylphosphine; palladium diacetate; In tetrahydrofuran; methanol; N,N-dimethyl-formamide;
DOI:10.1021/jo00037a047

Reference yield:

: 141019-26-3
diethyl N-<4-(2-formylethyl)benzoyl>-L-glutamate

: 141019-30-9
diethyl N-<4-<3-<<2-(pivaloylamino)-6-chloropyrimidin-4-yl>amino>propyl>benzoyl>-L-glutamate

Guidance literature:: Multi-step reaction with 5 steps

1: 93 percent / NaBH₄ / methanol / 1 h / 25 °C

2: 94 percent / TEA / tetrahydrofuran / 3 h / 25 °C

3: 93 percent / NaN₃ / dimethylformamide / 18 h / 25 °C

4: 95 percent / water, Ph₃P, / 18 h / 25 °C

5: 82 percent / TEA / tetrahydrofuran / 2 h / 25 °C

With sodium tetrahydroborate; sodium azide; TEA; water; triphenylphosphine; In tetrahydrofuran; methanol; N,N-dimethyl-formamide;
DOI:10.1021/jo00037a047