Hydrochloric Acid → HCID 22476022, compound
Reaction equation
C1(=O)N[C:4](=[O:6])[C:3]2=[CH:7][CH:8]=[CH:9][CH:10]=[C:2]12.NN.Cl.N[CH2:16][C:17]1[CH:18]=[N:19]C(C#N)=N[CH:22]=1.Cl>>[NH2:19][CH2:18][C:17]1[CH:16]=[CH:22][C:17]([C:18]#[N:19])=[CH:16][C:22]=1[O:6][CH2:4][C:3]1[CH:2]=[CH:10][CH:9]=[CH:8][CH:7]=1Participants
5
Procedure
Synthesis took place via the stage of the corresponding phthalimide as in Example 3.(f). The hydrazine cleavage was carried out as in Example 3.(g). The free amine was generated at pH 9-10 from the initially produced hydrochloride and was extracted from the aqueous solution with ether. 1H-NMR (DMSO-d6, δ in ppm): 7.65-7.25 (8H), 5.20 (s, 2H), 3.80 (s, 2H), ca. 3.0 (broad signal, NH2)
Workup
- customSynthesis
- extractionwas extracted from the aqueous solution with ether
Sources & evidence
- ORD record
- ord-5ee5a461058244ecbaab1baf4939c131
- Source dataset
- uspto-grants-2000_02
- Patent number
- US06030972
Reaction notes
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