(3-iodo-phenyl)-(7-methoxymethyl-7,8-dihydro-[1,4]dioxino[2,3-g]quinazolin-4-yl)-amine

Base Information

Chemical Name:(3-iodo-phenyl)-(7-methoxymethyl-7,8-dihydro-[1,4]dioxino[2,3-g]quinazolin-4-yl)-amine
CAS No.:489453-50-1
Molecular Formula:C₁₈H₁₆IN₃O₃
Molecular Weight:449.248
Hs Code.:

(3-iodo-phenyl)-(7-methoxymethyl-7,8-dihydro-[1,4]dioxino[2,3-<i>g</i>]quinazolin-4-yl)-amine

Synonyms:(3-iodo-phenyl)-(7-methoxymethyl-7,8-dihydro-[1,4]dioxino[2,3-g]quinazolin-4-yl)-amine

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Chemical Property of (3-iodo-phenyl)-(7-methoxymethyl-7,8-dihydro-[1,4]dioxino[2,3-g]quinazolin-4-yl)-amine

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Technology Process of (3-iodo-phenyl)-(7-methoxymethyl-7,8-dihydro-[1,4]dioxino[2,3-g]quinazolin-4-yl)-amine

There total 8 articles about (3-iodo-phenyl)-(7-methoxymethyl-7,8-dihydro-[1,4]dioxino[2,3-g]quinazolin-4-yl)-amine 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: 94.0%

: 626-01-7
3-Iodoaniline

: 489453-45-4
4-chloro-7-(methoxymethyl)-7,8-dihydro-[1,4]dioxino[2,3-g]quinazoline

: 489453-50-1
(3-iodo-phenyl)-(7-methoxymethyl-7,8-dihydro-[1,4]dioxino[2,3-g]quinazolin-4-yl)-amine

Guidance literature:: With hydrogenchloride; In isopropyl alcohol; for 24h; Heating;
DOI:10.1002/ardp.200290003

Reference yield:

: 20094-51-3
2-methoxymethyl-2,3-dihydro-benzo[1,4]dioxine

: 489453-50-1
(3-iodo-phenyl)-(7-methoxymethyl-7,8-dihydro-[1,4]dioxino[2,3-g]quinazolin-4-yl)-amine

Guidance literature:: Multi-step reaction with 7 steps

1.1: AlCl₃; N,N-dimethylacetamide / 0.25 h / 20 °C

1.2: 5 h / 20 °C

2.1: 48 percent / aq. NaOCl / 0.5 h / 65 °C

3.1: 54 percent / H₂SO₄; HNO₃ / acetic acid / 0.5 h / 20 °C

4.1: 65 percent / H₂ / 10 percent Pd/C / methanol / 24 h / 20 °C

5.1: 63 percent / piperidine / methanol / 4 h / Heating

6.1: 90 percent / POCl₃; N,N-dimethylaniline / 2 h / Heating

7.1: 94 percent / conc. HCl / propan-2-ol / 24 h / Heating

With piperidine; hydrogenchloride; sodium hypochlorite; aluminium trichloride; N,N-dimethyl acetamide; sulfuric acid; hydrogen; nitric acid; N,N-dimethyl-aniline; trichlorophosphate; palladium on activated charcoal; In methanol; acetic acid; isopropyl alcohol; 1.1: Friedel-Crafts acylation;
DOI:10.1002/ardp.200290003

Reference yield:

: 225927-73-1
7-acetyl-2-methoxymethyl-2,3-dihydro-benzo[1,4]dioxine

: 489453-50-1
(3-iodo-phenyl)-(7-methoxymethyl-7,8-dihydro-[1,4]dioxino[2,3-g]quinazolin-4-yl)-amine

Guidance literature:: Multi-step reaction with 6 steps

1: 48 percent / aq. NaOCl / 0.5 h / 65 °C

2: 54 percent / H₂SO₄; HNO₃ / acetic acid / 0.5 h / 20 °C

3: 65 percent / H₂ / 10 percent Pd/C / methanol / 24 h / 20 °C

4: 63 percent / piperidine / methanol / 4 h / Heating

5: 90 percent / POCl₃; N,N-dimethylaniline / 2 h / Heating

6: 94 percent / conc. HCl / propan-2-ol / 24 h / Heating

With piperidine; hydrogenchloride; sodium hypochlorite; sulfuric acid; hydrogen; nitric acid; N,N-dimethyl-aniline; trichlorophosphate; palladium on activated charcoal; In methanol; acetic acid; isopropyl alcohol;
DOI:10.1002/ardp.200290003