4,5-Dibromo-2-Pyrrolic Acid → HCID 58748174, compound

HRID 1162666Notes

Reaction equation

HRID 1162666 reaction equation
[NH2:1][CH2:2][C@H:3]1[CH2:7][CH2:6][N:5]([C:8]([O:10][C:11]([CH3:14])([CH3:13])[CH3:12])=[O:9])[CH2:4]1.[Br:15][C:16]1[CH:17]=[C:18]([C:22](O)=[O:23])[NH:19][C:20]=1[Br:21]>>[C:11]([O:10][C:8]([N:5]1[CH2:6][CH2:7][C@H:3]([CH2:2][NH:1][C:22]([C:18]2[NH:19][C:20]([Br:21])=[C:16]([Br:15])[CH:17]=2)=[O:23])[CH2:4]1)=[O:9])([CH3:14])([CH3:13])[CH3:12]

Participants

3

Procedure

60.1 Using general procedure E, (R)-3-aminomethyl-1-N-tert-butoxycarbonyl-pyrrolidine was coupled with 4,5-dibromo-1H-pyrrole-2-carboxylic acid to give (R)-3-{[(4,5-dibromo-1H-pyrrole-2-carbonyl)-amino]-methyl}-pyrrolidine-1-carboxylic acid tert-butyl ester. Pale yellow solid. MS449.9 ([M−H]−)

Sources & evidence

ORD record
ord-fb5e73ee45854abeb3c5dbbd6fb28b8f
Source dataset
uspto-grants-2010_10
Patent number
US07820699B2

Reaction notes

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