Hydrochloric Acid → HCID 70503709, compound
Reaction equation
[N:1]1([CH2:6][CH2:7][CH2:8][CH2:9][NH:10][C:11]2[C:20]3[CH2:19][CH2:18][CH2:17][CH2:16][C:15]=3[C:14]3=[N:21][N:22]=[CH:23][N:13]3[N:12]=2)[CH2:5][CH2:4][CH2:3][CH2:2]1.[ClH:24]>C(Cl)Cl>[ClH:24].[N:1]1([CH2:6][CH2:7][CH2:8][CH2:9][NH:10][C:11]2[C:20]3[CH2:19][CH2:18][CH2:17][CH2:16][C:15]=3[C:14]3=[N:21][N:22]=[CH:23][N:13]3[N:12]=2)[CH2:2][CH2:3][CH2:4][CH2:5]1.[ClH:24].[ClH:24].[N:1]1([CH2:6][CH2:7][CH2:8][CH2:9][NH:10][C:11]2[C:20]3[CH2:19][CH2:18][CH2:17][CH2:16][C:15]=3[C:14]3=[N:21][N:22]=[CH:23][N:13]3[N:12]=2)[CH2:2][CH2:3][CH2:4][CH2:5]1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
The amine obtained above was dissolved in methylene chloride and then treated with an excess of ethereal hydrogen chloride to give 6-[4-(1-pyrrolidinyl)butylamino]-7,8,9,10-tetrahydro-1,2,4-triazolo[3,4-a]phthalazine sesquihydrochloride melting at about 237°-238° C.
Sources & evidence
- ORD record
- ord-2b9683180833409ebef2119eb6405377
- Source dataset
- uspto-grants-1984_12
- Patent number
- US04487930
Reaction notes
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