4-Hydroxypyrrolidine → HCID 11408212, compound

HRID 1663142Notes

Reaction equation

HRID 1663142 reaction equation
[N:1]1[CH:6]=[CH:5][C:4]([CH2:7][NH:8][C:9]2[CH:28]=[CH:27][CH:26]=[CH:25][C:10]=2[C:11]([NH:13][O:14][CH2:15][C:16]2[CH:17]=[C:18]([CH:22]=[CH:23][CH:24]=2)[C:19](O)=[O:20])=[O:12])=[CH:3][CH:2]=1.[NH:29]1[CH2:33][CH2:32][CH:31]([OH:34])[CH2:30]1>>[OH:34][CH:31]1[CH2:32][CH2:33][N:29]([C:19]([C:18]2[CH:17]=[C:16]([CH:24]=[CH:23][CH:22]=2)[CH2:15][O:14][NH:13][C:11](=[O:12])[C:10]2[CH:25]=[CH:26][CH:27]=[CH:28][C:9]=2[NH:8][CH2:7][C:4]2[CH:5]=[CH:6][N:1]=[CH:2][CH:3]=2)=[O:20])[CH2:30]1

Participants

3

Procedure

Prepared by a similar procedure as described for preparation of example 405. Starting materials: 3-{2-[(Pyridin-4-ylmethyl)-amino]-benzoylaminooxymethyl}-benzoic acid (see example 403) and 3-pyrrolidinol (Aldrich).

Workup

  1. customPrepared by a similar procedure
  2. customas described for preparation of example 405

Sources & evidence

ORD record
ord-5cb5df39f5c6407a90cb46bcbd3d236d
Source dataset
uspto-grants-2011_10
Patent number
US08034811B2

Reaction notes

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