5-<4--(2S)-pyrrolidin-2-ylmethoxy>phenylmethyl>-2-imino-4-thiazolidinone

Base Information

Chemical Name:5-<4--(2S)-pyrrolidin-2-ylmethoxy>phenylmethyl>-2-imino-4-thiazolidinone
CAS No.:224954-16-9
Molecular Formula:C₃₆H₄₃N₃O₄S
Molecular Weight:613.821
Hs Code.:

5-<4-<N-<(3R/S)-2,3-dihydro-5-benzyloxy-2,2,4,6,7-pentamethylbenzofuran-3-ylmethyl>-(2S)-pyrrolidin-2-ylmethoxy>phenylmethyl>-2-imino-4-thiazolidinone

Synonyms:5-<4--(2S)-pyrrolidin-2-ylmethoxy>phenylmethyl>-2-imino-4-thiazolidinone

Suppliers and Price of 5-<4--(2S)-pyrrolidin-2-ylmethoxy>phenylmethyl>-2-imino-4-thiazolidinone

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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 5-<4--(2S)-pyrrolidin-2-ylmethoxy>phenylmethyl>-2-imino-4-thiazolidinone

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Technology Process of 5-<4--(2S)-pyrrolidin-2-ylmethoxy>phenylmethyl>-2-imino-4-thiazolidinone

There total 7 articles about 5-<4--(2S)-pyrrolidin-2-ylmethoxy>phenylmethyl>-2-imino-4-thiazolidinone 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: 87.0%

: 17356-08-0
thiourea

: 199109-36-9
ethyl 2-bromo-3-<4--(2S)-pyrrolidin-2-ylmethoxy>phenyl>propanoate

: 224954-16-9
5-<4--(2S)-pyrrolidin-2-ylmethoxy>phenylmethyl>-2-imino-4-thiazolidinone

Guidance literature:: With sodium acetate; In ethanol; for 12h; Heating;
DOI:10.1021/jm980549x

Reference yield:

: 350-46-9,178603-76-4
4-Fluoronitrobenzene

: 224954-16-9
5-<4--(2S)-pyrrolidin-2-ylmethoxy>phenylmethyl>-2-imino-4-thiazolidinone

Guidance literature:: Multi-step reaction with 4 steps

1: 1.) NaH / 1.) DMF, 25 deg C, 1 h, 2.) DMF, 25 deg C, 3 h

2: 55 percent / H₂ / 10 percent Pd/C / ethyl acetate / 48 h / 3102.89 Torr / Ambient temperature

3: 1.) NaNO₂, aq. HBr, 2.) Cu₂O / 1.) methanol, acetone, 5 deg C, 30 min, 2.) methanol, acetone, 38 deg C

4: 87 percent / sodium acetate / ethanol / 12 h / Heating

With copper(I) oxide; hydrogen bromide; hydrogen; sodium acetate; sodium hydride; sodium nitrite; palladium on activated charcoal; In ethanol; ethyl acetate;
DOI:10.1021/jm980549x

Reference yield:

: 183142-41-8
5-benzyloxy-2,2,4,6,7-pentamethyl-1-benzofuran-3-carbinol

: 224954-16-9
5-<4--(2S)-pyrrolidin-2-ylmethoxy>phenylmethyl>-2-imino-4-thiazolidinone

Guidance literature:: Multi-step reaction with 6 steps

1: 99 percent / Et₃N / CH₂Cl₂ / 3 h / 25 °C

2: 73 percent / 12 h / 120 °C

3: 1.) NaH / 1.) DMF, 25 deg C, 1 h, 2.) DMF, 25 deg C, 3 h

4: 55 percent / H₂ / 10 percent Pd/C / ethyl acetate / 48 h / 3102.89 Torr / Ambient temperature

5: 1.) NaNO₂, aq. HBr, 2.) Cu₂O / 1.) methanol, acetone, 5 deg C, 30 min, 2.) methanol, acetone, 38 deg C

6: 87 percent / sodium acetate / ethanol / 12 h / Heating

With copper(I) oxide; hydrogen bromide; hydrogen; sodium acetate; sodium hydride; triethylamine; sodium nitrite; palladium on activated charcoal; In ethanol; dichloromethane; ethyl acetate;
DOI:10.1021/jm980549x