1-[(2,2-difluorocyclopropyl)methyl]-3-methyl-5-[2-methyl-5-(piperazin-1-ylmethyl)phenyl]-1,3-dihydro[1,2,5]thiadiazolo[3,4-b]pyridine 2,2-dioxide

Base Information

Chemical Name:1-[(2,2-difluorocyclopropyl)methyl]-3-methyl-5-[2-methyl-5-(piperazin-1-ylmethyl)phenyl]-1,3-dihydro[1,2,5]thiadiazolo[3,4-b]pyridine 2,2-dioxide
CAS No.:1333264-79-1
Molecular Formula:C₂₂H₂₇F₂N₅O₂S
Molecular Weight:463.551
Hs Code.:

Synonyms:1-[(2,2-difluorocyclopropyl)methyl]-3-methyl-5-[2-methyl-5-(piperazin-1-ylmethyl)phenyl]-1,3-dihydro[1,2,5]thiadiazolo[3,4-b]pyridine 2,2-dioxide

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Chemical Property of 1-[(2,2-difluorocyclopropyl)methyl]-3-methyl-5-[2-methyl-5-(piperazin-1-ylmethyl)phenyl]-1,3-dihydro[1,2,5]thiadiazolo[3,4-b]pyridine 2,2-dioxide

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Technology Process of 1-[(2,2-difluorocyclopropyl)methyl]-3-methyl-5-[2-methyl-5-(piperazin-1-ylmethyl)phenyl]-1,3-dihydro[1,2,5]thiadiazolo[3,4-b]pyridine 2,2-dioxide

There total 5 articles about 1-[(2,2-difluorocyclopropyl)methyl]-3-methyl-5-[2-methyl-5-(piperazin-1-ylmethyl)phenyl]-1,3-dihydro[1,2,5]thiadiazolo[3,4-b]pyridine 2,2-dioxide 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:

: 1333264-78-0
tert-butyl 4-(3-{1-[(2,2-difluorocyclopropyl)methyl]-3-methyl-2,2-dioxido-1,3-dihydro[1,2,5]thiadiazolo[3,4-b]pyridin-5-yl}-4-methylbenzyl)piperazine-1-carboxylate

: 1333264-79-1
1-[(2,2-difluorocyclopropyl)methyl]-3-methyl-5-[2-methyl-5-(piperazin-1-ylmethyl)phenyl]-1,3-dihydro[1,2,5]thiadiazolo[3,4-b]pyridine 2,2-dioxide

Guidance literature:: With trifluoroacetic acid; In dichloromethane; at 20 ℃; for 0.75h;

Reference yield:

: 882679-40-5
methyl 4-methyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoate

: 1333264-79-1
1-[(2,2-difluorocyclopropyl)methyl]-3-methyl-5-[2-methyl-5-(piperazin-1-ylmethyl)phenyl]-1,3-dihydro[1,2,5]thiadiazolo[3,4-b]pyridine 2,2-dioxide

Guidance literature:: Multi-step reaction with 4 steps

1.1: potassium phosphate; 2-dicyclohexylphosphino-2′,6′-dimethoxybiphenyl / palladium diacetate / water; tetrahydrofuran / 14 h / 75 °C

2.1: diisobutylaluminium hydride / n-heptane; tetrahydrofuran / -78 °C

3.1: triethylamine; methanesulfonyl chloride / 1-methyl-pyrrolidin-2-one / 0.33 h

3.2: 2 h / 80 °C

4.1: trifluoroacetic acid / dichloromethane / 0.75 h / 20 °C

With potassium phosphate; 2-dicyclohexylphosphino-2′,6′-dimethoxybiphenyl; diisobutylaluminium hydride; methanesulfonyl chloride; triethylamine; trifluoroacetic acid; palladium diacetate; In tetrahydrofuran; 1-methyl-pyrrolidin-2-one; n-heptane; dichloromethane; water;

Reference yield:

: 1333263-97-0
5-chloro-1-1-[(2,2-difluorocyclopropyl)methyl]-3-methyl-1,3-dihydro-[1,2,5]thiadiazolo[3,4-b]pyridine-2,2-dioxide

: 1333264-79-1
1-[(2,2-difluorocyclopropyl)methyl]-3-methyl-5-[2-methyl-5-(piperazin-1-ylmethyl)phenyl]-1,3-dihydro[1,2,5]thiadiazolo[3,4-b]pyridine 2,2-dioxide

Guidance literature:: Multi-step reaction with 4 steps

1.1: potassium phosphate; 2-dicyclohexylphosphino-2′,6′-dimethoxybiphenyl / palladium diacetate / water; tetrahydrofuran / 14 h / 75 °C

2.1: diisobutylaluminium hydride / n-heptane; tetrahydrofuran / -78 °C

3.1: triethylamine; methanesulfonyl chloride / 1-methyl-pyrrolidin-2-one / 0.33 h

3.2: 2 h / 80 °C

4.1: trifluoroacetic acid / dichloromethane / 0.75 h / 20 °C

With potassium phosphate; 2-dicyclohexylphosphino-2′,6′-dimethoxybiphenyl; diisobutylaluminium hydride; methanesulfonyl chloride; triethylamine; trifluoroacetic acid; palladium diacetate; In tetrahydrofuran; 1-methyl-pyrrolidin-2-one; n-heptane; dichloromethane; water;