2-Aminothiophenol → HCID 66759823, compound

HRID 1402940Notes

Reaction equation

HRID 1402940 reaction equation
[NH2:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[SH:8].[Cl:9][C:10]1[CH:15]=[CH:14][C:13]([CH:16]2[CH2:22][C:21](=O)[O:20][C:18](=[O:19])[CH2:17]2)=[CH:12][CH:11]=1>>[S:8]1[C:3]2[CH:4]=[CH:5][CH:6]=[CH:7][C:2]=2[N:1]=[C:21]1[CH2:22][CH:16]([C:13]1[CH:12]=[CH:11][C:10]([Cl:9])=[CH:15][CH:14]=1)[CH2:17][C:18]([OH:20])=[O:19]

Participants

3

Reactant 2

HCID 87132-AminothiophenolHCID 1046394-(4-Chlorophenyl)dihydro-2H-pyran-2,6(3H)-dione

Product 1

HCID 66759823HCID 66759823, compound

Procedure

By a procedure similar to that of example 1.55, starting from 2-aminothiophenol and 3-(4-chlorophenyl)glutaric anhydride, 4-(2-benzothiazolyl)-3-(4-chlorophenyl)-butanoic acid was obtained as colourless solid.

Sources & evidence

ORD record
ord-af1ff609938d4b31a7c4e0e9bf0a6d2b
Source dataset
uspto-grants-2014_12
Patent number
US08912186B2

Reaction notes

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