(5-methoxycarbonylamino-[1,2,4]thiadiazol-3-yl)-(Z)-trityloxyimino-acetic acid methyl ester

Base Information

Chemical Name:(5-methoxycarbonylamino-[1,2,4]thiadiazol-3-yl)-(Z)-trityloxyimino-acetic acid methyl ester
CAS No.:620967-17-1
Molecular Formula:C₂₆H₂₂N₄O₅S
Molecular Weight:502.55
Hs Code.:

Synonyms:(5-methoxycarbonylamino-[1,2,4]thiadiazol-3-yl)-(Z)-trityloxyimino-acetic acid methyl ester

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Chemical Property of (5-methoxycarbonylamino-[1,2,4]thiadiazol-3-yl)-(Z)-trityloxyimino-acetic acid methyl ester

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Technology Process of (5-methoxycarbonylamino-[1,2,4]thiadiazol-3-yl)-(Z)-trityloxyimino-acetic acid methyl ester

There total 5 articles about (5-methoxycarbonylamino-[1,2,4]thiadiazol-3-yl)-(Z)-trityloxyimino-acetic acid methyl 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: 62.0%

: 76-83-5
trityl chloride

: 149196-72-5
(Z)-hydroxyimino-(5-methoxycarbonylamino-[1,2,4]thiadiazol-3-yl)-acetic acid methyl ester

: 620967-17-1
(5-methoxycarbonylamino-[1,2,4]thiadiazol-3-yl)-(Z)-trityloxyimino-acetic acid methyl ester

Guidance literature:: With triethylamine; In dichloromethane; at 0 ℃; for 2h;
DOI:10.1016/S0968-0896(02)00431-5

Reference yield:

: 157251-67-7
(5-methoxycarbonylamino-[1,2,4]thiadiazol-3-yl)-acetic acid

: 620967-17-1
(5-methoxycarbonylamino-[1,2,4]thiadiazol-3-yl)-(Z)-trityloxyimino-acetic acid methyl ester

Guidance literature:: Multi-step reaction with 5 steps

1: 98 percent / thionyl cloride / 16 h / 20 °C

2: bromine / methanol; CH₂Cl₂ / 0 - 20 °C

3: pyridine-N-oxide / acetonitrile / 1 h / Heating

4: hydroxylamine hydrochloride / ethanol / 16 h / 20 °C

5: 62 percent / Et₃N / CH₂Cl₂ / 2 h / 0 °C

With pyridine N-oxide; thionyl chloride; hydroxylamine hydrochloride; bromine; triethylamine; In methanol; ethanol; dichloromethane; acetonitrile;
DOI:10.1016/S0968-0896(02)00431-5

Reference yield:

: 149196-71-4
(5-methoxycarbonylamino-[1,2,4]thiadiazol-3-yl)-acetic acid methyl ester

: 620967-17-1
(5-methoxycarbonylamino-[1,2,4]thiadiazol-3-yl)-(Z)-trityloxyimino-acetic acid methyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: bromine / methanol; CH₂Cl₂ / 0 - 20 °C

2: pyridine-N-oxide / acetonitrile / 1 h / Heating

3: hydroxylamine hydrochloride / ethanol / 16 h / 20 °C

4: 62 percent / Et₃N / CH₂Cl₂ / 2 h / 0 °C

With pyridine N-oxide; hydroxylamine hydrochloride; bromine; triethylamine; In methanol; ethanol; dichloromethane; acetonitrile;
DOI:10.1016/S0968-0896(02)00431-5