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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Propanol, reaction products with ammonia, distn. residuesHCID 18331942—
Reactant7-[chloro(1-methyl-1H-imidazol-5-yl)(4-methylphenyl)methyl]-5-(3-chlorophenyl)-tetrazolo[1,5-a]quinazoline. hydrochlorideHCID 131727375—
SolventTetrahydrofuranHCID 8028—
Product5-(3-Chlorophenyl)-alpha-(1-methyl-1h-imidazol-5-yl)-alpha-(4-methylphenyl)-tetrazolo[1,5-a]quinazoline-7-methanamineHCID 6868733933%

Reaction Conditions

Temperature5 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07655654B2
Source datasetuspto-grants-2010_02
ORD IDord-73dbfff319604bad9649169bd73c0bc6
Source noteuspto-grants-2010_02