HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1441475Generated: November 1, 2026
2-Propanol, reaction products with ammonia, distn. residues → 5-(3-Chlorophenyl)-alpha-(1-methyl-1h-imidazol-5-yl)-alpha-(4-methylphenyl)-tetrazolo[1,5-a]quinazoline-7-methanamine
https://huagongshe.com/reaction/1441475
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Propanol, reaction products with ammonia, distn. residues | HCID 18331942 | — |
| Reactant | 7-[chloro(1-methyl-1H-imidazol-5-yl)(4-methylphenyl)methyl]-5-(3-chlorophenyl)-tetrazolo[1,5-a]quinazoline. hydrochloride | HCID 131727375 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 5-(3-Chlorophenyl)-alpha-(1-methyl-1h-imidazol-5-yl)-alpha-(4-methylphenyl)-tetrazolo[1,5-a]quinazoline-7-methanamine | HCID 68687339 | 33% |
Reaction Steps
A mixture of intermediate 26 (0.0083 mol) in THF (80 ml) was cooled to 5° C. under N2 flow. NH3/iPrOH (80 ml ) was added dropwise. The mixture was stirred at 5° C. for 1 hours, then brought to room temperature. The mixture was stirred at room temperature overnight, poured out into ice water and extracted with DCM. The organic layer was separated, washed with water, dried (MgSO4), filtered and the solvent was evaporated. The residue was purified by column chromatography over silica gel (15-40 μm) (eluent: DCM/MeOH/NH4OH 96/4/0.2). The pure fractions were collected and the solvent was evaporated. The residue was crystallized from CH3CN. The precipitate was filtered off and dried, yielding 1.37 g (33%) of 5-(3-chlorophenyl)-α-(1-methyl-1H-imidazol-5-yl)-α-(4—methylphenyl)-tetrazolo[1,5-a]quinazoline-7-methanamine .hydrate (1:1) (intermediate 27), mp. 150° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07655654B2 |
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| Source dataset | uspto-grants-2010_02 |
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| ORD ID | ord-73dbfff319604bad9649169bd73c0bc6 |
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| Source note | uspto-grants-2010_02 |
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