N-benzyloxycarbonyl-4-methoxycarbonylmethylamino-L-proline tert-butyl ester

Base Information

Chemical Name:N-benzyloxycarbonyl-4-methoxycarbonylmethylamino-L-proline tert-butyl ester
CAS No.:224321-03-3
Molecular Formula:C₂₀H₂₈N₂O₆
Molecular Weight:392.452
Hs Code.:

Synonyms:N-benzyloxycarbonyl-4-methoxycarbonylmethylamino-L-proline tert-butyl ester

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Chemical Property of N-benzyloxycarbonyl-4-methoxycarbonylmethylamino-L-proline tert-butyl ester

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Technology Process of N-benzyloxycarbonyl-4-methoxycarbonylmethylamino-L-proline tert-butyl ester

There total 3 articles about N-benzyloxycarbonyl-4-methoxycarbonylmethylamino-L-proline 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:

Reference yield:

: 64187-47-9
1-benzyloxycarbonyl-4-keto-L-proline

: 224321-03-3
N-benzyloxycarbonyl-4-methoxycarbonylmethylamino-L-proline tert-butyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 79 percent / 70 percent HClO₄ / 28 h / 11 °C

2: 1.) 1 N NaOH, 2.) NaBH₃CN / 1.) MeOH, 17 deg C, 30 min, 2.) MeOH, 17 deg C, 80 min

With sodium hydroxide; perchloric acid; sodium cyanoborohydride;

Reference yield:

: 13504-85-3
(2S,4R)-1-(benzyloxycarbonyl)-4-hydroxypyrrolidine-2-carboxylic acid

: 224321-03-3
N-benzyloxycarbonyl-4-methoxycarbonylmethylamino-L-proline tert-butyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 2.67 M CrO₃, 8 N H₂SO₄ / acetone / Ambient temperature

2: 79 percent / 70 percent HClO₄ / 28 h / 11 °C

3: 1.) 1 N NaOH, 2.) NaBH₃CN / 1.) MeOH, 17 deg C, 30 min, 2.) MeOH, 17 deg C, 80 min

With chromium(VI) oxide; sodium hydroxide; perchloric acid; sulfuric acid; sodium cyanoborohydride; In acetone;

Reference yield:

: 5680-79-5,883886-67-7
glycine ethyl ester hydrochloride

: 147489-27-8
(2S)-4-oxo-1-phenylmethoxycarbonylpyrrolidine-2-carboxylic acid tert-butyl ester

: 224321-03-3
N-benzyloxycarbonyl-4-methoxycarbonylmethylamino-L-proline tert-butyl ester

Guidance literature:: With sodium hydroxide; sodium cyanoborohydride; Yield given; Multistep reaction; 1.) MeOH, 17 deg C, 30 min, 2.) MeOH, 17 deg C, 80 min;