Hydrochloric Acid → HCID 18173116, compound
Reaction equation
[O:1]=[C:2]1[CH2:7][CH:6]2[CH:8]([C:9](O)=O)[CH:3]1[CH2:4][CH2:5]2.[CH2:12]([N:15]1[C:22]([NH2:23])=[C:21]([NH2:24])[C:19](=[O:20])[N:18]([CH2:25][CH2:26][CH3:27])[C:16]1=[O:17])[CH2:13][CH3:14].Cl>>[O:1]=[C:2]1[CH2:7][CH:6]2[CH:8]([C:9]3[NH:24][C:21]4[C:19](=[O:20])[N:18]([CH2:25][CH2:26][CH3:27])[C:16](=[O:17])[N:15]([CH2:12][CH2:13][CH3:14])[C:22]=4[N:23]=3)[CH:3]1[CH2:4][CH2:5]2Participants
4
Procedure
2-Oxo-bicyclo[2.2.1]heptane-7-carboxylic acid (308 mg) was couple to 1,3-Dipropyl-5,6-diaminouracil.HCl (576 mg) and cyclized using the procedures from Example 1. Yield: 320 mg. Mass (ES+ 345).
Sources & evidence
- ORD record
- ord-90b96fc01ddc464ebd17552d276968c7
- Source dataset
- uspto-grants-2003_08
- Patent number
- US06605600B1
Reaction notes
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