Isopropylamine → HCID 136377093, compound
Reaction equation
CO[C:3]([C:5]1[N:6]=[C:7]([CH2:13][C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][C:15]=2[Br:20])[NH:8][C:9](=[O:12])[C:10]=1[OH:11])=[O:4].[CH:21]([NH2:24])([CH3:23])[CH3:22]>>[CH:21]([NH:24][C:3]([C:5]1[N:6]=[C:7]([CH2:13][C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][C:15]=2[Br:20])[NH:8][C:9](=[O:12])[C:10]=1[OH:11])=[O:4])([CH3:23])[CH3:22]Participants
3
Procedure
The compound was prepared according to the same procedure as in Example 21 using 2-(2-bromo-benzyl)-5-hydroxy-6-oxo-1,6-dihydro-pyrimidine-4-carboxylic acid methyl ester (0.08 g; 0.236 mmol) and isopropylamine (0.4 ml; 4.7 mmol). This gave the title compound as a white solid (0.021 g; 24%). LCMS: m/z=367 (MH+).
Workup
- customThe compound was prepared
Sources & evidence
- ORD record
- ord-c34713f0d0534ce7b34f267634c6ae6d
- Source dataset
- uspto-grants-2014_12
- Patent number
- US08921388B2
Reaction notes
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