2-(1-chloroethyl)-5-methyl-3-phenylpyrrolo[1,2-f][1,2,4]triazin-4(3H)-one

Base Information

Chemical Name:2-(1-chloroethyl)-5-methyl-3-phenylpyrrolo[1,2-f][1,2,4]triazin-4(3H)-one
CAS No.:1403942-35-7
Molecular Formula:C₁₅H₁₄ClN₃O
Molecular Weight:287.749
Hs Code.:

Synonyms:2-(1-chloroethyl)-5-methyl-3-phenylpyrrolo[1,2-f][1,2,4]triazin-4(3H)-one

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Chemical Property of 2-(1-chloroethyl)-5-methyl-3-phenylpyrrolo[1,2-f][1,2,4]triazin-4(3H)-one

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Technology Process of 2-(1-chloroethyl)-5-methyl-3-phenylpyrrolo[1,2-f][1,2,4]triazin-4(3H)-one

There total 1 articles about 2-(1-chloroethyl)-5-methyl-3-phenylpyrrolo[1,2-f][1,2,4]triazin-4(3H)-one 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: 18.0%

: 7623-09-8
2-chloropropionyl chloride

: 1403942-32-4
1-amino-3-methyl-N-phenyl-1H-pyrrole-2-carboxamide

: 1403942-35-7
2-(1-chloroethyl)-5-methyl-3-phenylpyrrolo[1,2-f][1,2,4]triazin-4(3H)-one

Guidance literature:: 2-chloropropionyl chloride; 1-amino-3-methyl-N-phenyl-1H-pyrrole-2-carboxamide; With acetic acid; at 20 ℃; for 1h;

With trichlorophosphate; for 16h; Reflux;

With ammonia; In methanol; at 60 ℃; Sealed;

Reference yield: 94.0%

: 1403942-35-7
2-(1-chloroethyl)-5-methyl-3-phenylpyrrolo[1,2-f][1,2,4]triazin-4(3H)-one

: 1403942-37-9
2-(1-iodoethyl)-5-methyl-3-phenylpyrrolo[1,2-f][1,2,4]triazin-4(3H)-one

Guidance literature:: With sodium iodide; In acetone; at 20 - 65 ℃;

Reference yield:

: 1403942-35-7
2-(1-chloroethyl)-5-methyl-3-phenylpyrrolo[1,2-f][1,2,4]triazin-4(3H)-one

: 1403946-11-1
2-(1-(6-amino-9H-purin-9-yl)ethyl)-5-methyl-3-phenylpyrrolo[2,1-f][1,2,4]triazin-4(3H)-one

Guidance literature:: Multi-step reaction with 2 steps

1: sodium iodide / acetone / 20 - 65 °C

2: potassium carbonate / N,N-dimethyl-formamide / 50 °C

With potassium carbonate; sodium iodide; In N,N-dimethyl-formamide; acetone;