2-methoxy-3-[2-[3-(thiazol-2-ylaminomethyl)-benzoylamino]-2-(2,9,9-trimethyl-3,5-dioxa-4-bora-tricyclo[6.1.1.0(2,6)]dec-4-yl)-ethyl]-benzoic acid tert-butyl ester

Base Information

Chemical Name:2-methoxy-3-[2-[3-(thiazol-2-ylaminomethyl)-benzoylamino]-2-(2,9,9-trimethyl-3,5-dioxa-4-bora-tricyclo[6.1.1.0(2,6)]dec-4-yl)-ethyl]-benzoic acid tert-butyl ester
CAS No.:1256336-84-1
Molecular Formula:C₃₅H₄₄BN₃O₆S
Molecular Weight:645.628
Hs Code.:

2-methoxy-3-[2-[3-(thiazol-2-ylaminomethyl)-benzoylamino]-2-(2,9,9-trimethyl-3,5-dioxa-4-bora-tricyclo[6.1.1.0(2,6)]dec-4-yl)-ethyl]-benzoic acid tert-butyl ester

Synonyms:2-methoxy-3-[2-[3-(thiazol-2-ylaminomethyl)-benzoylamino]-2-(2,9,9-trimethyl-3,5-dioxa-4-bora-tricyclo[6.1.1.0(2,6)]dec-4-yl)-ethyl]-benzoic acid tert-butyl ester

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Chemical Property of 2-methoxy-3-[2-[3-(thiazol-2-ylaminomethyl)-benzoylamino]-2-(2,9,9-trimethyl-3,5-dioxa-4-bora-tricyclo[6.1.1.0(2,6)]dec-4-yl)-ethyl]-benzoic acid tert-butyl ester

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Technology Process of 2-methoxy-3-[2-[3-(thiazol-2-ylaminomethyl)-benzoylamino]-2-(2,9,9-trimethyl-3,5-dioxa-4-bora-tricyclo[6.1.1.0(2,6)]dec-4-yl)-ethyl]-benzoic acid tert-butyl ester

There total 7 articles about 2-methoxy-3-[2-[3-(thiazol-2-ylaminomethyl)-benzoylamino]-2-(2,9,9-trimethyl-3,5-dioxa-4-bora-tricyclo[6.1.1.0(2,6)]dec-4-yl)-ethyl]-benzoic 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: 28.0%

: 96-50-4
2-thiazolylamine

: 1256336-65-8
3-[2-(3-formyl-benzoylamino)-2-(2,9,9-trimethyl-3,5-doxa-4-bora-tricyclo[6.1.1.0.(2,6)]dec-4-yl)-ethyl]-2-methoxy-benzoic acid tert-butyl ester

: 1256336-84-1
2-methoxy-3-[2-[3-(thiazol-2-ylaminomethyl)-benzoylamino]-2-(2,9,9-trimethyl-3,5-dioxa-4-bora-tricyclo[6.1.1.0(2,6)]dec-4-yl)-ethyl]-benzoic acid tert-butyl ester

Guidance literature:: 2-thiazolylamine; 3-[2-(3-formyl-benzoylamino)-2-(2,9,9-trimethyl-3,5-doxa-4-bora-tricyclo[6.1.1.0.(2,6)]dec-4-yl)-ethyl]-2-methoxy-benzoic acid tert-butyl ester; With acetic acid; In methanol; at 20 ℃; for 25.5h; Sonographic reaction;

With methanol; sodium tetrahydroborate; for 1h;

Reference yield:

: 913836-10-9
3-(dihydroxyboranyl)-2-methoxybenzoic acid

: 1256336-84-1
2-methoxy-3-[2-[3-(thiazol-2-ylaminomethyl)-benzoylamino]-2-(2,9,9-trimethyl-3,5-dioxa-4-bora-tricyclo[6.1.1.0(2,6)]dec-4-yl)-ethyl]-benzoic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 6 steps

1.1: sulfuric acid / 1,4-dioxane; water / 18 h / 0 - 20 °C / Sealed tube

2.1: tetrahydrofuran / 1 h / 20 °C

3.1: n-butyllithium / tetrahydrofuran; hexane / -100 °C / Inert atmosphere

4.1: n-butyllithium / tetrahydrofuran; hexane / 0.5 h / -100 °C / Inert atmosphere

4.2: -100 - 0 °C / Inert atmosphere

4.3: -78 - 20 °C / Inert atmosphere

5.1: pyridine / 2.75 h / -78 - 20 °C

6.1: acetic acid / methanol / 25.5 h / 20 °C / Sonographic reaction

6.2: 1 h

With pyridine; n-butyllithium; acetic acid; sulfuric acid; In tetrahydrofuran; 1,4-dioxane; methanol; hexane; water;

Reference yield:

: 619-21-6
m-formylphenyl benzoic acid

: 1256336-84-1
2-methoxy-3-[2-[3-(thiazol-2-ylaminomethyl)-benzoylamino]-2-(2,9,9-trimethyl-3,5-dioxa-4-bora-tricyclo[6.1.1.0(2,6)]dec-4-yl)-ethyl]-benzoic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 3 steps

1.1: oxalyl dichloride / N,N-dimethyl-formamide / dichloromethane / 0.08 h / -20 °C / Inert atmosphere

2.1: pyridine / 2.75 h / -78 - 20 °C

3.1: acetic acid / methanol / 25.5 h / 20 °C / Sonographic reaction

3.2: 1 h

With pyridine; oxalyl dichloride; acetic acid; N,N-dimethyl-formamide; In methanol; dichloromethane;