Acetone → HCID 22647883, compound

HRID 394125Notes

Reaction equation

[CH:1]12[CH2:7][CH:4]([NH:5][CH2:6]1)[CH2:3][N:2]2[C:8]([O:10][C:11]([CH3:14])([CH3:13])[CH3:12])=[O:9].[CH3:15][C:16]([CH3:18])=O>>[CH:16]([N:5]1[CH2:6][CH:1]2[CH2:7][CH:4]1[CH2:3][N:2]2[C:8]([O:10][C:11]([CH3:14])([CH3:13])[CH3:12])=[O:9])([CH3:18])[CH3:15]

Participants

Reactant 2

HCID 180Acetone

HCID 2760898(1S,4S)-tert-butyl 2,5-diazabicyclo(2.2.1)heptane-2-carboxylate

Product 1

HCID 22647883HCID 22647883, compound

Procedure

The title compound was prepared from tert-butyl 2,5-diazabicyclo[2.2.1]heptane-2-carboxylate and using acetone as described in EXAMPLE AAA1, Step A.

Sources & evidence

ORD record: ord-406fd4daf8394f27bc458700bbb0d94c
Source dataset: uspto-grants-2004_10
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US06809199B2

Reaction notes

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