(4-amino-phenyl)-(5-pyridin-2-ylmethyl-2,3,4,5-tetrahydro-benzo[b][1,4]diazepin-1-yl)-methanone

Base Information

Chemical Name:(4-amino-phenyl)-(5-pyridin-2-ylmethyl-2,3,4,5-tetrahydro-benzo[b][1,4]diazepin-1-yl)-methanone
CAS No.:159588-62-2
Molecular Formula:C₂₂H₂₂N₄O
Molecular Weight:358.443
Hs Code.:

(4-amino-phenyl)-(5-pyridin-2-ylmethyl-2,3,4,5-tetrahydro-benzo[<i>b</i>][1,4]diazepin-1-yl)-methanone

Synonyms:(4-amino-phenyl)-(5-pyridin-2-ylmethyl-2,3,4,5-tetrahydro-benzo[b][1,4]diazepin-1-yl)-methanone

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Chemical Property of (4-amino-phenyl)-(5-pyridin-2-ylmethyl-2,3,4,5-tetrahydro-benzo[b][1,4]diazepin-1-yl)-methanone

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Technology Process of (4-amino-phenyl)-(5-pyridin-2-ylmethyl-2,3,4,5-tetrahydro-benzo[b][1,4]diazepin-1-yl)-methanone

There total 5 articles about (4-amino-phenyl)-(5-pyridin-2-ylmethyl-2,3,4,5-tetrahydro-benzo[b][1,4]diazepin-1-yl)-methanone 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: 76.0%

: 159588-59-7
1-(4-nitrobenzoyl)-5-(2-pyridylmethyl)-2,3,4,5-tetrahydro-1H-1,5-benzodiazepine

: 159588-62-2
(4-amino-phenyl)-(5-pyridin-2-ylmethyl-2,3,4,5-tetrahydro-benzo[b][1,4]diazepin-1-yl)-methanone

Guidance literature:: With tin(ll) chloride; In ethyl acetate; for 1.5h; Heating;
DOI:10.1248/cpb.46.1566

Reference yield:

: 5755-07-7
2,3,4,5-tetrahydro-1H-1,5-benzodiazepin-2-one

: 159588-62-2
(4-amino-phenyl)-(5-pyridin-2-ylmethyl-2,3,4,5-tetrahydro-benzo[b][1,4]diazepin-1-yl)-methanone

Guidance literature:: Multi-step reaction with 4 steps

1: 1.) NaH / 1.) DMF, from 0 deg C to 20 deg C, 20 min, 2.) DMF, from 0 deg C to 5 deg C, 1.5 h

2: 36 percent / BH₃*THF / tetrahydrofuran / 5 h / Heating

3: 88 percent / Et₃N / CH₂Cl₂ / 1 h / 0 - 5 °C

4: 76 percent / SnCl₂*H₂O / ethyl acetate / 1.5 h / Heating

With borane-THF; sodium hydride; triethylamine; tin(ll) chloride; In tetrahydrofuran; dichloromethane; ethyl acetate;
DOI:10.1248/cpb.46.1566

Reference yield:

: 6959-47-3
2-chloromethylpyridine hydrochloride

: 159588-62-2
(4-amino-phenyl)-(5-pyridin-2-ylmethyl-2,3,4,5-tetrahydro-benzo[b][1,4]diazepin-1-yl)-methanone

Guidance literature:: Multi-step reaction with 4 steps

1: 1.) NaH / 1.) DMF, from 0 deg C to 20 deg C, 20 min, 2.) DMF, from 0 deg C to 5 deg C, 1.5 h

2: 36 percent / BH₃*THF / tetrahydrofuran / 5 h / Heating

3: 88 percent / Et₃N / CH₂Cl₂ / 1 h / 0 - 5 °C

4: 76 percent / SnCl₂*H₂O / ethyl acetate / 1.5 h / Heating

With borane-THF; sodium hydride; triethylamine; tin(ll) chloride; In tetrahydrofuran; dichloromethane; ethyl acetate;
DOI:10.1248/cpb.46.1566