1-[3,5-bis(trifluoromethyl)phenyl]-3-[(1S,2S)-2-{[2-({[3,5-bis(trifluoromethyl)phenyl]carbamothioyl}amino)phenyl]sulfanyl}cyclohexyl]thiourea

Base Information

Chemical Name:1-[3,5-bis(trifluoromethyl)phenyl]-3-[(1S,2S)-2-{[2-({[3,5-bis(trifluoromethyl)phenyl]carbamothioyl}amino)phenyl]sulfanyl}cyclohexyl]thiourea
CAS No.:1351099-63-2
Molecular Formula:C₃₀H₂₄F₁₂N₄S₃
Molecular Weight:764.726
Hs Code.:

1-[3,5-bis(trifluoromethyl)phenyl]-3-[(1S,2S)-2-{[2-({[3,5-bis(trifluoromethyl)phenyl]carbamothioyl}amino)phenyl]sulfanyl}cyclohexyl]thiourea

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Chemical Property of 1-[3,5-bis(trifluoromethyl)phenyl]-3-[(1S,2S)-2-{[2-({[3,5-bis(trifluoromethyl)phenyl]carbamothioyl}amino)phenyl]sulfanyl}cyclohexyl]thiourea

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Technology Process of 1-[3,5-bis(trifluoromethyl)phenyl]-3-[(1S,2S)-2-{[2-({[3,5-bis(trifluoromethyl)phenyl]carbamothioyl}amino)phenyl]sulfanyl}cyclohexyl]thiourea

There total 3 articles about 1-[3,5-bis(trifluoromethyl)phenyl]-3-[(1S,2S)-2-{[2-({[3,5-bis(trifluoromethyl)phenyl]carbamothioyl}amino)phenyl]sulfanyl}cyclohexyl]thiourea 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:

: 1072-86-2,1460-57-7,1792-81-0,54383-22-1,57794-08-8,931-17-9
(1R,2R)-trans-1,2-cyclohexanediol

: 1351099-63-2
1-[3,5-bis(trifluoromethyl)phenyl]-3-[(1S,2S)-2-{[2-({[3,5-bis(trifluoromethyl)phenyl]carbamothioyl}amino)phenyl]sulfanyl}cyclohexyl]thiourea

Guidance literature:: Multi-step reaction with 4 steps

1: tributylphosphine / toluene / 80 °C / Inert atmosphere

2: hydrogen azide; triphenylphosphine; diethylazodicarboxylate / toluene; benzene / 24 h / Inert atmosphere

3: methanol; triphenylphosphine / 2 h / Reflux

4: dichloromethane / 20 °C / Inert atmosphere

With methanol; hydrogen azide; tributylphosphine; triphenylphosphine; diethylazodicarboxylate; In dichloromethane; toluene; benzene; 2: Mitsunobu reaction / 3: Staudinger reaction;
DOI:10.1016/j.tetasy.2011.09.015

Reference yield:

: 1141-88-4
2-Aminophenyl disulfide

: 1351099-63-2
1-[3,5-bis(trifluoromethyl)phenyl]-3-[(1S,2S)-2-{[2-({[3,5-bis(trifluoromethyl)phenyl]carbamothioyl}amino)phenyl]sulfanyl}cyclohexyl]thiourea

Guidance literature:: Multi-step reaction with 4 steps

1: tributylphosphine / toluene / 80 °C / Inert atmosphere

2: hydrogen azide; triphenylphosphine; diethylazodicarboxylate / toluene; benzene / 24 h / Inert atmosphere

3: methanol; triphenylphosphine / 2 h / Reflux

4: dichloromethane / 20 °C / Inert atmosphere

With methanol; hydrogen azide; tributylphosphine; triphenylphosphine; diethylazodicarboxylate; In dichloromethane; toluene; benzene; 2: Mitsunobu reaction / 3: Staudinger reaction;
DOI:10.1016/j.tetasy.2011.09.015

Reference yield:

: 1351099-44-9
(-)-(1R,2S)-2-(2-aminophenylsulfanyl)cyclohexanol

: 1351099-63-2
1-[3,5-bis(trifluoromethyl)phenyl]-3-[(1S,2S)-2-{[2-({[3,5-bis(trifluoromethyl)phenyl]carbamothioyl}amino)phenyl]sulfanyl}cyclohexyl]thiourea

Guidance literature:: Multi-step reaction with 3 steps

1: hydrogen azide; triphenylphosphine; diethylazodicarboxylate / toluene; benzene / 24 h / Inert atmosphere

2: methanol; triphenylphosphine / 2 h / Reflux

3: dichloromethane / 20 °C / Inert atmosphere

With methanol; hydrogen azide; triphenylphosphine; diethylazodicarboxylate; In dichloromethane; toluene; benzene; 1: Mitsunobu reaction / 2: Staudinger reaction;
DOI:10.1016/j.tetasy.2011.09.015