(S)-tert-butyl 3-(((S)-1-(((S)-1-(hydroxyamino)-1-oxo-3-phenylpropan-2-yl)amino)-1-oxo-3-phenylpropan-2-yl)carbamoyl)-3,4-dihydroisoquinoline-2(1H)-carboxylate

Base Information

Chemical Name:(S)-tert-butyl 3-(((S)-1-(((S)-1-(hydroxyamino)-1-oxo-3-phenylpropan-2-yl)amino)-1-oxo-3-phenylpropan-2-yl)carbamoyl)-3,4-dihydroisoquinoline-2(1H)-carboxylate
CAS No.:1338587-29-3
Molecular Formula:C₃₃H₃₈N₄O₆
Molecular Weight:586.688
Hs Code.:

(S)-tert-butyl 3-(((S)-1-(((S)-1-(hydroxyamino)-1-oxo-3-phenylpropan-2-yl)amino)-1-oxo-3-phenylpropan-2-yl)carbamoyl)-3,4-dihydroisoquinoline-2(1H)-carboxylate

Synonyms:(S)-tert-butyl 3-(((S)-1-(((S)-1-(hydroxyamino)-1-oxo-3-phenylpropan-2-yl)amino)-1-oxo-3-phenylpropan-2-yl)carbamoyl)-3,4-dihydroisoquinoline-2(1H)-carboxylate

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Chemical Property of (S)-tert-butyl 3-(((S)-1-(((S)-1-(hydroxyamino)-1-oxo-3-phenylpropan-2-yl)amino)-1-oxo-3-phenylpropan-2-yl)carbamoyl)-3,4-dihydroisoquinoline-2(1H)-carboxylate

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Technology Process of (S)-tert-butyl 3-(((S)-1-(((S)-1-(hydroxyamino)-1-oxo-3-phenylpropan-2-yl)amino)-1-oxo-3-phenylpropan-2-yl)carbamoyl)-3,4-dihydroisoquinoline-2(1H)-carboxylate

There total 4 articles about (S)-tert-butyl 3-(((S)-1-(((S)-1-(hydroxyamino)-1-oxo-3-phenylpropan-2-yl)amino)-1-oxo-3-phenylpropan-2-yl)carbamoyl)-3,4-dihydroisoquinoline-2(1H)-carboxylate 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: 40.2%

: 1338587-06-6
(S)-tert-butyl 3-(((S)-1-(((S)-1-methoxy-1-oxo-3-phenylpropan-2-yl)amino)-1-oxo-3-phenylpropan-2-yl)carbamoyl)-3,4-dihydroisoquinoline-2(1H)-carboxylate

: 1338587-29-3
(S)-tert-butyl 3-(((S)-1-(((S)-1-(hydroxyamino)-1-oxo-3-phenylpropan-2-yl)amino)-1-oxo-3-phenylpropan-2-yl)carbamoyl)-3,4-dihydroisoquinoline-2(1H)-carboxylate

Guidance literature:: With methanol; hydroxylamine potassium salt; at 20 ℃; for 12h;
DOI:10.1016/j.bmc.2011.08.041

Reference yield:

: 115962-35-1,144069-68-1,78879-20-6
(3S)-2-tert-butoxycarbonyl-1,2,3,4-tetrahydroisoquinole-3-carboxylic acid

: 1338587-29-3
(S)-tert-butyl 3-(((S)-1-(((S)-1-(hydroxyamino)-1-oxo-3-phenylpropan-2-yl)amino)-1-oxo-3-phenylpropan-2-yl)carbamoyl)-3,4-dihydroisoquinoline-2(1H)-carboxylate

Guidance literature:: Multi-step reaction with 2 steps

1: dmap; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine / dichloromethane / 12.5 h / 0 - 20 °C

2: methanol; hydroxylamine potassium salt / 12 h / 20 °C

With methanol; dmap; hydroxylamine potassium salt; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; In dichloromethane;
DOI:10.1016/j.bmc.2011.08.041

Reference yield:

: 63-91-2,25191-15-5,658-69-5,67675-33-6
L-phenylalanine

: 1338587-29-3
(S)-tert-butyl 3-(((S)-1-(((S)-1-(hydroxyamino)-1-oxo-3-phenylpropan-2-yl)amino)-1-oxo-3-phenylpropan-2-yl)carbamoyl)-3,4-dihydroisoquinoline-2(1H)-carboxylate

Guidance literature:: Multi-step reaction with 4 steps

1: hydrogenchloride / water / 90 °C

2: sodium hydroxide

3: dmap; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine / dichloromethane / 12.5 h / 0 - 20 °C

4: methanol; hydroxylamine potassium salt / 12 h / 20 °C

With hydrogenchloride; methanol; dmap; hydroxylamine potassium salt; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; sodium hydroxide; In dichloromethane; water; 1: Pictet-Spengler cyclisation;
DOI:10.1016/j.bmc.2011.08.041