3-(2,4-Dichlorophenyl)propanoic acid → HCID 58295760, compound

HRID 390191Notes

Reaction equation

HRID 390191 reaction equation
[Cl:1][C:2]1[CH:7]=[C:6]([Cl:8])[CH:5]=[CH:4][C:3]=1[CH2:9][CH2:10][C:11]([OH:13])=O.[Cl:14][C:15]1[CH:16]=[CH:17][CH:18]=[C:19]2[C:28]=1[C:22]1([CH2:27][CH2:26][NH:25][CH2:24][CH2:23]1)[CH2:21][CH:20]2[CH2:29][C:30]([O:32]CC)=[O:31]>>[Cl:14][C:15]1[CH:16]=[CH:17][CH:18]=[C:19]2[C:28]=1[C:22]1([CH2:23][CH2:24][N:25]([C:11](=[O:13])[CH2:10][CH2:9][C:3]3[CH:4]=[CH:5][C:6]([Cl:8])=[CH:7][C:2]=3[Cl:1])[CH2:26][CH2:27]1)[CH2:21][CH:20]2[CH2:29][C:30]([OH:32])=[O:31]

Participants

3

Reactant 2

HCID 27409153-(2,4-Dichlorophenyl)propanoic acidHCID 67224803Ethyl 2-(7-chloro-2,3-dihydrospiro[indene-1,4'-piperidine]-3-yl)acetate

Product 1

HCID 58295760HCID 58295760, compound

Procedure

The title compound was prepared following a procedure analogous to that described in Example 1 using 3-(2,4-dichlorophenyl)propanoic acid and ethyl 2-(7-chloro-2,3-dihydrospiro[indene-1,4′-piperidine]-3-yl)acetate followed by a procedure analogous to that in Example 2. LC-MS Method 1 tR=2.03, min, m/z=484, 482, 480

Sources & evidence

ORD record
ord-1f8933e2767d4e9eba80aaa3a1bb842b
Source dataset
uspto-grants-2013_02
Patent number
US08383629B2

Reaction notes

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