diphenyl N-benzyloxycarbonylamino-(4-(N,N'-bis(tert-butyloxycarbonyl)guanyl)butyl)methanephosphonate

Base Information

Chemical Name:diphenyl N-benzyloxycarbonylamino-(4-(N,N'-bis(tert-butyloxycarbonyl)guanyl)butyl)methanephosphonate
CAS No.:695171-99-4
Molecular Formula:C₃₆H₄₇N₄O₉P
Molecular Weight:710.764
Hs Code.:

Synonyms:diphenyl N-benzyloxycarbonylamino-(4-(N,N'-bis(tert-butyloxycarbonyl)guanyl)butyl)methanephosphonate

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Chemical Property of diphenyl N-benzyloxycarbonylamino-(4-(N,N'-bis(tert-butyloxycarbonyl)guanyl)butyl)methanephosphonate

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Technology Process of diphenyl N-benzyloxycarbonylamino-(4-(N,N'-bis(tert-butyloxycarbonyl)guanyl)butyl)methanephosphonate

There total 7 articles about diphenyl N-benzyloxycarbonylamino-(4-(N,N'-bis(tert-butyloxycarbonyl)guanyl)butyl)methanephosphonate 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: 8.0%

: 149194-47-8
(5-Amino-1-benzyloxycarbonylamino-pentyl)-phosphonic acid diphenyl ester

: 152120-54-2,862686-58-6,1143572-00-2
(Z)-tert-butyl (((tert-butoxycarbonyl)imino)(1H-pyrazol-1-yl)methyl)carbamate

: 695171-99-4
diphenyl N-benzyloxycarbonylamino-(4-(N,N'-bis(tert-butyloxycarbonyl)guanyl)butyl)methanephosphonate

Guidance literature:: With TEA; In acetonitrile; at 20 ℃;
DOI:10.1021/jm0499209

Reference yield:

: 101-02-0
triphenyl phosphite

: 695171-99-4
diphenyl N-benzyloxycarbonylamino-(4-(N,N'-bis(tert-butyloxycarbonyl)guanyl)butyl)methanephosphonate

Guidance literature:: Multi-step reaction with 3 steps

1: 45 percent / acetic acid / 2 h / 90 °C

2: NH₂NH₂*H₂O / tetrahydrofuran

3: 8 percent / TEA / acetonitrile / 20 °C

With TEA; hydrazine hydrate; acetic acid; In tetrahydrofuran; acetonitrile;
DOI:10.1021/jm0499209

Reference yield:

: 2508-29-4
5-hydroxypentylamine

: 695171-99-4
diphenyl N-benzyloxycarbonylamino-(4-(N,N'-bis(tert-butyloxycarbonyl)guanyl)butyl)methanephosphonate

Guidance literature:: Multi-step reaction with 5 steps

1: triethylamine / toluene / 3 h / 125 °C

2: 77 percent / oxalyl chloride; DMSO; diisopropylethylamine / CH₂Cl₂ / -78 - 20 °C

3: 45 percent / acetic acid / 2 h / 90 °C

4: NH₂NH₂*H₂O / tetrahydrofuran

5: 8 percent / TEA / acetonitrile / 20 °C

With oxalyl dichloride; TEA; hydrazine hydrate; acetic acid; dimethyl sulfoxide; triethylamine; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; dichloromethane; toluene; acetonitrile; 2: Swern oxidation;
DOI:10.1021/jm0499209