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CAS 147255-16-1

(4R)-4-(3,4-Dichlorophenyl)-4-phenylbutanoic acid

Codes:Sertraline Hydrochloride-066

Application context (from source-drug indications)

强迫性障碍枸橼酸舍曲林

Source drugs (routes using this intermediate)

DrugTierExpiry
枸橼酸舍曲林Sertraline CitrateTier C — Watch / trade-

Position in synthesis routes (up/downstream chain)

Ordered by route registration; left → right is the synthesis direction. The highlighted node is the current CAS; others link to their own profiles.

枸橼酸舍曲林优化路线steps: 5total yield: /
(4R)-4-(3,4-Dichlorophenyl)-4-phenylbutanoic acid→4-(3,4-Dichlorophenyl)-4-phenylbutanoyl chloride→Carbamic acid methyl ester→methyl N-[4-(3,4-dichlorophenyl)-4-phenylbutanoyl]carbamate→methyl N-[4-(3,4-dichlorophenyl)-1-hydroxy-4-phenylbutyl]carbamate→Ethyl [(1S,4S)-4-(3,4-dichlorophenyl)-1,2,3,4-tetrahydronaphthalen-1-yl]carbamate
枸橼酸舍曲林优化路线steps: 5total yield: /
Ethenylbenzene→Methyl (3E)-2-diazo-4-phenylbut-3-enoate→methyl (2S)-2-phenyl-1-[(E)-2-phenylethenyl]cyclopropane-1-carboxylate→1,1-dimethyl (2S)-2-phenylcyclopropane-1,1-dicarboxylate→3,4-Dichlorotoluene→1,3-dimethyl 2-[(2R)-2-(3,4-dichlorophenyl)-2-phenylethyl]propanedioate→(4R)-4-(3,4-Dichlorophenyl)-4-phenylbutanoic acid→4(S)-(3,4-Dichlorophenyl)-1,2,3,4-tetrahydronaphthalen-1-one
枸橼酸舍曲林优化路线steps: 6total yield: /
(3,4-Dichlorophenyl)(phenyl)methanone→Butane-1,4-dioic acid diethyl diester→ethyl (3E)-4-(3,4-dichlorophenyl)-4-phenylbut-3-enoate→(2E)-4-(3,4-Dichlorophenyl)-4-phenylbut-2-enoic acid→(3E)-4-(3,4-dichlorophenyl)-4-phenylbut-3-enoate; 2-methylpropan-2-aminium→(4R)-4-(3,4-dichlorophenyl)-4-phenylbutanoate; 2-methylpropan-2-aminium→(4R)-4-(3,4-Dichlorophenyl)-4-phenylbutanoic acid→4(S)-(3,4-Dichlorophenyl)-1,2,3,4-tetrahydronaphthalen-1-one
枸橼酸舍曲林优化路线steps: 8total yield: /
4-(3,4-Dichlorophenyl)-4-oxobutanoic acid→4-(3,4-Dichlorophenyl)-4-hydroxybutanoic acid→(5R)-5-(3,4-Dichlorophenyl)oxolan-2-one→(1R)-1-(3,4-Dichlorophenyl)butane-1,4-diol→(1R)-1-(3,4-Dichlorophenyl)-4-[[(2,3,3-trimethylbutan-2-yl)silyl]oxy]butan-1-ol→(4R)-4-(3,4-Dichlorophenyl)-4-phenylbutanoic acid→(1R)-1-(3,4-Dichlorophenyl)-4-[[(2,3,3-trimethylbutan-2-yl)silyl]oxy]butyl methanesulfonate→Phenyllithium→[(4R)-4-(3,4-Dichlorophenyl)-4-phenylbutoxy](2,3,3-trimethylbutan-2-yl)silane→(4R)-4-(3,4-Dichlorophenyl)-4-phenylbutan-1-ol

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