(3RS)-3-benzyloxycarbonylamino-1-cyclohexyl-carbonylmethyl-2,3-dihydro-5-isobutyl-9-methyl-1H-1,4-benzodiazepin-2-one

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Chemical Name:(3RS)-3-benzyloxycarbonylamino-1-cyclohexyl-carbonylmethyl-2,3-dihydro-5-isobutyl-9-methyl-1H-1,4-benzodiazepin-2-one
CAS No.:205998-75-0
Molecular Formula:C₃₀H₃₇N₃O₄
Molecular Weight:503.641
Hs Code.:

Synonyms:(3RS)-3-benzyloxycarbonylamino-1-cyclohexyl-carbonylmethyl-2,3-dihydro-5-isobutyl-9-methyl-1H-1,4-benzodiazepin-2-one

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Chemical Property of (3RS)-3-benzyloxycarbonylamino-1-cyclohexyl-carbonylmethyl-2,3-dihydro-5-isobutyl-9-methyl-1H-1,4-benzodiazepin-2-one

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Technology Process of (3RS)-3-benzyloxycarbonylamino-1-cyclohexyl-carbonylmethyl-2,3-dihydro-5-isobutyl-9-methyl-1H-1,4-benzodiazepin-2-one

There total 7 articles about (3RS)-3-benzyloxycarbonylamino-1-cyclohexyl-carbonylmethyl-2,3-dihydro-5-isobutyl-9-methyl-1H-1,4-benzodiazepin-2-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: 77.8%

: 56077-28-2
Bromomethyl cyclohexyl ketone

: 205996-00-5
(3RS)-3-benzyloxycarbonylamino-2,3-dihydro-5-isobutyl-9-methyl-1H-1,4-benzodiazepin-2-one

: 205998-75-0
(3RS)-3-benzyloxycarbonylamino-1-cyclohexyl-carbonylmethyl-2,3-dihydro-5-isobutyl-9-methyl-1H-1,4-benzodiazepin-2-one

Guidance literature:: (3RS)-3-benzyloxycarbonylamino-2,3-dihydro-5-isobutyl-9-methyl-1H-1,4-benzodiazepin-2-one; With sodium hydride; In N,N-dimethyl-formamide; at 0 - 20 ℃; for 4h;

Bromomethyl cyclohexyl ketone; In N,N-dimethyl-formamide; at 20 ℃; for 5.5h;
DOI:10.1248/cpb.48.1

Reference yield:

: 625-28-5
Isovaleronitrile

: 205998-75-0
(3RS)-3-benzyloxycarbonylamino-1-cyclohexyl-carbonylmethyl-2,3-dihydro-5-isobutyl-9-methyl-1H-1,4-benzodiazepin-2-one

Guidance literature:: Multi-step reaction with 4 steps

1.1: BCl₃ / toluene / 1 h / 20 °C

1.2: AlCl₃ / acetonitrile / 5 h / Heating

1.3: 100 percent / 2 N aq. HCl / acetonitrile / 2.5 h / Heating

2.1: N-methylmorpholine / tetrahydrofuran / 0 - 20 °C

3.1: NH₃ / methanol / 20 °C

4.1: NaH / dimethylformamide / 4 h / 0 - 20 °C

4.2: 77.8 percent / dimethylformamide / 5.5 h / 20 °C

With 4-methyl-morpholine; ammonia; boron trichloride; sodium hydride; In tetrahydrofuran; methanol; N,N-dimethyl-formamide; toluene; 1.1: Addition / 1.2: Rearrangement / 1.3: Hydrolysis / 2.1: Acylation / 3.1: Cyclization / 4.1: deprotonation / 4.2: Alkylation;
DOI:10.1248/cpb.48.1

Reference yield:

: 124676-19-3
2-(benzotriazol-1-yl)-N-(benzyloxycarbonyl)glycine

: 205998-75-0
(3RS)-3-benzyloxycarbonylamino-1-cyclohexyl-carbonylmethyl-2,3-dihydro-5-isobutyl-9-methyl-1H-1,4-benzodiazepin-2-one

Guidance literature:: Multi-step reaction with 4 steps

1.1: (COCl)2; DMF / tetrahydrofuran / 2 h / 0 °C

2.1: N-methylmorpholine / tetrahydrofuran / 0 - 20 °C

3.1: NH₃ / methanol / 20 °C

4.1: NaH / dimethylformamide / 4 h / 0 - 20 °C

4.2: 77.8 percent / dimethylformamide / 5.5 h / 20 °C

With 4-methyl-morpholine; oxalyl dichloride; ammonia; sodium hydride; N,N-dimethyl-formamide; In tetrahydrofuran; methanol; N,N-dimethyl-formamide; 1.1: Chlorination / 2.1: Acylation / 3.1: Cyclization / 4.1: deprotonation / 4.2: Alkylation;
DOI:10.1248/cpb.48.1