1-Pyrrolidineethanamine → HCID 58990036, compound
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.[NH2:29][CH2:30][CH2:31][N:32]1[CH2:36][CH2:35][CH2:34][CH2:33]1>>[N:32]1([CH2:31][CH2:30][NH: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:3]=[CH:2][N:1]=[CH:6][CH:5]=2)=[O:20])[CH2:36][CH2:35][CH2:34][CH2:33]1Participants
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 N-(2-aminoethyl)pyrrolidine (Aldrich).
Workup
- customPrepared by a similar procedure
- customas described for preparation of example 405
Sources & evidence
- ORD record
- ord-f780410c3b0b4159bf2e436ba5fd405b
- Source dataset
- uspto-grants-2011_10
- Patent number
- US08034811B2
Reaction notes
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