(6-amino-4-benzyloxy-1-iodo-naphthalen-2-yl)-(3-chloro-allyl)-carbamic acid tert-butyl ester

Base Information

Chemical Name:(6-amino-4-benzyloxy-1-iodo-naphthalen-2-yl)-(3-chloro-allyl)-carbamic acid tert-butyl ester
CAS No.:286374-28-5
Molecular Formula:C₂₅H₂₆ClIN₂O₃
Molecular Weight:564.851
Hs Code.:

(6-amino-4-benzyloxy-1-iodo-naphthalen-2-yl)-(3-chloro-allyl)-carbamic acid <i>tert</i>-butyl ester

Synonyms:(6-amino-4-benzyloxy-1-iodo-naphthalen-2-yl)-(3-chloro-allyl)-carbamic acid tert-butyl ester

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Chemical Property of (6-amino-4-benzyloxy-1-iodo-naphthalen-2-yl)-(3-chloro-allyl)-carbamic acid tert-butyl ester

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Technology Process of (6-amino-4-benzyloxy-1-iodo-naphthalen-2-yl)-(3-chloro-allyl)-carbamic acid tert-butyl ester

There total 8 articles about (6-amino-4-benzyloxy-1-iodo-naphthalen-2-yl)-(3-chloro-allyl)-carbamic acid tert-butyl ester 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:

: 222835-54-3
N-(tert-butyloxycarbonyl)-N-(3-chloro-2-propen-1-yl)-4-benzyloxy-1-iodo-6-nitro-2-naphthylamine

: 286374-28-5
(6-amino-4-benzyloxy-1-iodo-naphthalen-2-yl)-(3-chloro-allyl)-carbamic acid tert-butyl ester

Guidance literature:: With iron(III) chloride; hydrazine hydrate;
DOI:10.1039/a807884j

Reference yield:

: 222535-08-2
N-(tert-butyloxycarbonyl)-4-benzyloxy-1-iodo-6-nitro-2-naphthylamine

: 286374-28-5
(6-amino-4-benzyloxy-1-iodo-naphthalen-2-yl)-(3-chloro-allyl)-carbamic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 83 percent / NaH / dimethylformamide / 1 h

2: FeCl₃*6H₂O; N₂H₄*H₂O / methanol; tetrahydrofuran / 7 h / Heating

With iron(III) chloride; sodium hydride; hydrazine hydrate; In tetrahydrofuran; methanol; N,N-dimethyl-formamide; 1: deprotonation / 1: Alkylation / 2: Reduction;
DOI:10.1016/S0968-0896(00)00088-2

Reference yield:

: 79290-07-6
ethyl 4-hydroxy-6-nitro-2-naphthalenecarboxylate

: 286374-28-5
(6-amino-4-benzyloxy-1-iodo-naphthalen-2-yl)-(3-chloro-allyl)-carbamic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 6 steps

1: K₂CO₃; Bu₄NI / dimethylformamide / 10 h / 23 °C

2: 10.648 g / aq. LiOH / tetrahydrofuran; methanol; H₂O / 4 h / 23 °C

3: 84 percent / Et₃N; 4A MS; diphenyl phosphorazidate / 15 h / Heating

4: 98 percent / TsOH*H₂O; NIS / tetrahydrofuran; methanol / 4 h / -40 °C

5: 83 percent / NaH / dimethylformamide / 1 h

6: FeCl₃*6H₂O; N₂H₄*H₂O / methanol; tetrahydrofuran / 7 h / Heating

With lithium hydroxide; N-iodo-succinimide; diphenyl phosphoryl azide; iron(III) chloride; tetra-(n-butyl)ammonium iodide; sodium hydride; potassium carbonate; toluene-4-sulfonic acid; hydrazine hydrate; triethylamine; In tetrahydrofuran; methanol; water; N,N-dimethyl-formamide; 1: Alkylation / 2: Hydrolysis / 3: Curtius rearrangement / 4: Iodination / 5: deprotonation / 5: Alkylation / 6: Reduction;
DOI:10.1016/S0968-0896(00)00088-2