(S)-2-(1-aminoethyl)-5-chloro-3-phenylquinazolin-4(3H)-one 2,2,2-trifluoroacetic acid salt

Base Information

Chemical Name:(S)-2-(1-aminoethyl)-5-chloro-3-phenylquinazolin-4(3H)-one 2,2,2-trifluoroacetic acid salt
CAS No.:1615680-60-8
Molecular Formula:C₂HF₃O₂*C₁₆H₁₄ClN₃O
Molecular Weight:413.784
Hs Code.:

Synonyms:(S)-2-(1-aminoethyl)-5-chloro-3-phenylquinazolin-4(3H)-one 2,2,2-trifluoroacetic acid salt

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Chemical Property of (S)-2-(1-aminoethyl)-5-chloro-3-phenylquinazolin-4(3H)-one 2,2,2-trifluoroacetic acid salt

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Technology Process of (S)-2-(1-aminoethyl)-5-chloro-3-phenylquinazolin-4(3H)-one 2,2,2-trifluoroacetic acid salt

There total 3 articles about (S)-2-(1-aminoethyl)-5-chloro-3-phenylquinazolin-4(3H)-one 2,2,2-trifluoroacetic acid salt 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:

: 1441309-09-6
tert-butyl (S)-(1-(5-chloro-4-oxo-3-phenyl-3,4-dihydroquinazoline-2-yl)ethyl)carbamate

: 76-05-1
trifluoroacetic acid

: 1615680-60-8
(S)-2-(1-aminoethyl)-5-chloro-3-phenylquinazolin-4(3H)-one 2,2,2-trifluoroacetic acid salt

Guidance literature:: In dichloromethane; at 20 ℃; for 3h;

Reference yield:

: 2148-56-3
2-chloro-6-aminobenzoic acid

: 1615680-60-8
(S)-2-(1-aminoethyl)-5-chloro-3-phenylquinazolin-4(3H)-one 2,2,2-trifluoroacetic acid salt

Guidance literature:: Multi-step reaction with 3 steps

1: pyridine; diphenyl phosphite / 2 h / 40 °C

2: 12 h / 55 °C

3: dichloromethane / 3 h / 20 °C

With pyridine; diphenyl phosphite; In dichloromethane;
DOI:10.1021/acs.jmedchem.6b00213

Reference yield:

: C₁₅H₁₇ClN₂O₄

: 1615680-60-8
(S)-2-(1-aminoethyl)-5-chloro-3-phenylquinazolin-4(3H)-one 2,2,2-trifluoroacetic acid salt

Guidance literature:: Multi-step reaction with 2 steps

1: 12 h / 55 °C

2: dichloromethane / 3 h / 20 °C

In dichloromethane;
DOI:10.1021/acs.jmedchem.6b00213