1-(3-Aminopropyl)-2-pyrrolidinone → HCID 58149323, compound

HRID 563732Notes

Reaction equation

HRID 563732 reaction equation
[CH3:1][O:2][C:3](=[O:21])[CH2:4][C:5]1[CH:6]=[C:7]([C:11]2[C:16]([O:17][CH3:18])=[CH:15][CH:14]=[CH:13][C:12]=2[CH:19]=O)[CH:8]=[CH:9][CH:10]=1.[NH2:22][CH2:23][CH2:24][CH2:25][N:26]1[CH2:30][CH2:29][CH2:28][C:27]1=[O:31]>>[CH3:1][O:2][C:3](=[O:21])[CH2:4][C:5]1[CH:6]=[C:7]([C:11]2[C:16]([O:17][CH3:18])=[CH:15][CH:14]=[CH:13][C:12]=2[CH2:19][NH:22][CH2:23][CH2:24][CH2:25][N:26]2[CH2:30][CH2:29][CH2:28][C:27]2=[O:31])[CH:8]=[CH:9][CH:10]=1

Participants

3

Reactant 2

HCID 821111-(3-Aminopropyl)-2-pyrrolidinoneHCID 58149056HCID 58149056, compound

Product 1

HCID 58149323HCID 58149323, compound

Procedure

Prepared according to the procedure described in Example 33, Step 4, using the following starting materials: (2′-formyl-6′-methoxy-biphenyl-3-yl)-acetic acid methyl ester and 1-(3-aminopropyl)-2-pyrrolidinone.

Workup

  1. customPrepared

Sources & evidence

ORD record
ord-ab19fd7ddafe46128d719e7fc1217885
Source dataset
uspto-grants-2011_11
Patent number
US08067445B2

Reaction notes

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