Dimethylamine → HCID 67270559, compound

HRID 602492Notes

Reaction equation

[C:1]([O:5][C:6]([N:8]1[CH2:12][C@@H:11]([NH:13][C:14]([C:16]2[C:24]3[C:19](=[CH:20][CH:21]=[CH:22][CH:23]=3)[N:18]([CH:25]([CH3:27])[CH3:26])[N:17]=2)=[O:15])[CH2:10][C@H:9]1[CH2:28][O:29][CH2:30][C:31](O)=[O:32])=[O:7])([CH3:4])([CH3:3])[CH3:2].[CH3:34][NH:35][CH3:36]>>[CH3:34][N:35]([CH3:36])[C:31](=[O:32])[CH2:30][O:29][CH2:28][C@@H:9]1[CH2:10][C@H:11]([NH:13][C:14]([C:16]2[C:24]3[C:19](=[CH:20][CH:21]=[CH:22][CH:23]=3)[N:18]([CH:25]([CH3:26])[CH3:27])[N:17]=2)=[O:15])[CH2:12][N:8]1[C:6]([O:5][C:1]([CH3:2])([CH3:3])[CH3:4])=[O:7]

Participants

Reactant 2

HCID 674Dimethylamine

HCID 67271014HCID 67271014, compound

Product 1

HCID 67270559HCID 67270559, compound

Procedure

The title compound was prepared according to the procedure described in step 1 of Example 7 from [((2S,4S)-1-(tert-Butoxycarbonyl)-4-{[(1-isopropyl-1H-indazol-3-yl)carbonyl]amino}pyrrolidin-2-yl)methoxy]acetic acid (step 1 of Example 21) and dimethylamine.

Sources & evidence

ORD record: ord-46a70b819c6d4236b9c07431c2c0e5fc
Source dataset: uspto-grants-2011_03
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US07906532B2

Reaction notes

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