(S)-tert-butoxycarbonylamino[4-(3-pyridin-4-ylisoquinolin-1-yloxy)phenyl]acetic acid

Base Information

Chemical Name:(S)-tert-butoxycarbonylamino[4-(3-pyridin-4-ylisoquinolin-1-yloxy)phenyl]acetic acid
CAS No.:928162-17-8
Molecular Formula:C₂₇H₂₅N₃O₅
Molecular Weight:471.513
Hs Code.:

Synonyms:(S)-tert-butoxycarbonylamino[4-(3-pyridin-4-ylisoquinolin-1-yloxy)phenyl]acetic acid

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Chemical Property of (S)-tert-butoxycarbonylamino[4-(3-pyridin-4-ylisoquinolin-1-yloxy)phenyl]acetic acid

Chemical Property:

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Technology Process of (S)-tert-butoxycarbonylamino[4-(3-pyridin-4-ylisoquinolin-1-yloxy)phenyl]acetic acid

There total 2 articles about (S)-tert-butoxycarbonylamino[4-(3-pyridin-4-ylisoquinolin-1-yloxy)phenyl]acetic acid 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:

: 7742-73-6
1,3-dichloroisoquinoline

: 928162-17-8
(S)-tert-butoxycarbonylamino[4-(3-pyridin-4-ylisoquinolin-1-yloxy)phenyl]acetic acid

Guidance literature:: Multi-step reaction with 2 steps

1: 99 percent / potassium tert-butoxide / dimethylsulfoxide / 336 h / 40 °C

2: 31 percent / [(t-Bu)3PH]BF₄; KF / Pd₂(dba)3 / tetrahydrofuran / 0.25 h / 170 °C / microwave irradiation

With potassium fluoride; potassium tert-butylate; tri tert-butylphosphoniumtetrafluoroborate; tris(dibenzylideneacetone)dipalladium ⁽⁰⁾; In tetrahydrofuran; dimethyl sulfoxide; 2: Suzuki reaction;
DOI:10.1016/j.bmc.2006.11.003

Reference yield:

: 69651-48-5
N-tert-butyloxycarbonyl-L-4-hydroxyphenylglycine

: 928162-17-8
(S)-tert-butoxycarbonylamino[4-(3-pyridin-4-ylisoquinolin-1-yloxy)phenyl]acetic acid

Guidance literature:: Multi-step reaction with 2 steps

1: 99 percent / potassium tert-butoxide / dimethylsulfoxide / 336 h / 40 °C

2: 31 percent / [(t-Bu)3PH]BF₄; KF / Pd₂(dba)3 / tetrahydrofuran / 0.25 h / 170 °C / microwave irradiation

With potassium fluoride; potassium tert-butylate; tri tert-butylphosphoniumtetrafluoroborate; tris(dibenzylideneacetone)dipalladium ⁽⁰⁾; In tetrahydrofuran; dimethyl sulfoxide; 2: Suzuki reaction;
DOI:10.1016/j.bmc.2006.11.003

Reference yield: 40.0%

: 928162-17-8
(S)-tert-butoxycarbonylamino[4-(3-pyridin-4-ylisoquinolin-1-yloxy)phenyl]acetic acid

: 630421-49-7
(1R,2S)-1-amino-N-(cyclopropylsulfonyl)-2-vinylcyclopropanecarboxamide hydrochloride

: 928162-31-6
C₃₆H₃₇N₅O₇S

Guidance literature:: With N-ethyl-N,N-diisopropylamine; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate; In N,N-dimethyl-formamide; at 20 ℃; pH=10;
DOI:10.1016/j.bmc.2006.11.003