3-(4-fluorophenyl)-1-methylspiro<3H-indole-3,2'-thiazolidine>-2,4'(1H)-dione

Base Information

Chemical Name:3-(4-fluorophenyl)-1-methylspiro<3H-indole-3,2'-thiazolidine>-2,4'(1H)-dione
CAS No.:131141-18-9
Molecular Formula:C₁₇H₁₃FN₂O₂S
Molecular Weight:328.367
Hs Code.:

Synonyms:3-(4-fluorophenyl)-1-methylspiro<3H-indole-3,2'-thiazolidine>-2,4'(1H)-dione

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of 3-(4-fluorophenyl)-1-methylspiro<3H-indole-3,2'-thiazolidine>-2,4'(1H)-dione

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Technology Process of 3-(4-fluorophenyl)-1-methylspiro<3H-indole-3,2'-thiazolidine>-2,4'(1H)-dione

There total 5 articles about 3-(4-fluorophenyl)-1-methylspiro<3H-indole-3,2'-thiazolidine>-2,4'(1H)-dione 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: 88.0%

: 79962-58-6
3'-(4-fluorophenyl)spiro<3H-indole-3,2'-thiazolidine>-2,4'(1H)-dione

: 77-78-1
dimethyl sulfate

: 131141-18-9
3-(4-fluorophenyl)-1-methylspiro<3H-indole-3,2'-thiazolidine>-2,4'(1H)-dione

Guidance literature:: With potassium hydroxide; In ethanol; for 1h;

Reference yield:

: 2058-74-4
1-methyl-1H-indole-2,3-dione

: 131141-18-9
3-(4-fluorophenyl)-1-methylspiro<3H-indole-3,2'-thiazolidine>-2,4'(1H)-dione

Guidance literature:: Multi-step reaction with 3 steps

1: 89 percent / glacial acetic acid / ethanol / 0.5 h / Heating

2: 91 percent / toluene / 6 h

3: mercaptoacetic acid / toluene / 16 h / Ambient temperature

With acetic acid; mercaptoacetic acid; In ethanol; toluene;

Reference yield:

: 21231-47-0
3-((4-fluorophenyl)imino)indolin-2-one

: 131141-18-9
3-(4-fluorophenyl)-1-methylspiro<3H-indole-3,2'-thiazolidine>-2,4'(1H)-dione

Guidance literature:: Multi-step reaction with 3 steps

1: 10percent KOH / ethanol / 1 h

2: 91 percent / toluene / 6 h

3: mercaptoacetic acid / toluene / 16 h / Ambient temperature

With potassium hydroxide; mercaptoacetic acid; In ethanol; toluene;