HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1696561Generated: November 1, 2026
Stannous chloride dihydrate → HCID 136347864, compound
https://huagongshe.com/reaction/1696561
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Stannous chloride dihydrate | HCID 61436 | — |
| Reactant | Pentanenitrile, 4,4-dimethyl-3-oxo- | HCID 108871 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Reactant | 6-Amino-3,4-dihydroquinazolin-4-one | HCID 135478037 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 136347864 | HCID 136347864 | 22.3% |
Reaction Steps
To a suspension of 6-aminoquinazolin-4(3H)-one (3.07 g, 19.0 mmol, 1.0 eq) in conc. HCl (30.0 ml) at 0° C. was added dropwise NaNO2 (1.51 g, 21.9 mmol, 1.15 eq) as a solution in H2O (20.0 ml). The resulting mixture was stirred at 0° C. for 1 h, and then treated with a solution of SnCl2.2H2O (18.5 g, 81.9 mmol, 4.30 eq) in conc. HCl (20.0 ml). The reaction was stirred at 0° C. for 1 h and then at RT for 2 h. The reaction was diluted with EtOH (200 ml), treated with 4,4-dimethyl-3-oxopentanenitrile (3.10 g, 24.8 mmol, 1.30 eq), heated at reflux overnight, then cooled to RT and concentrated. The residue was diluted with EtOAc (100 mL), then stirred in an ice/H2O bath and made basic (pH 8) with solid NaOH. The mixture was filtered through Celite®, washed with H2O (50 mL) and then EtOAc (100 mL). The organic phase was washed with brine, dried (Na2SO4) and concentrated to yield a yellow solid, which was triturated from Et2O (100 ml) to yield 6-(5-amino-3-t-butyl-1H-pyrazol-1-yl)quinazolin-4(3H)-one (1.2 g, 22% yield). MS (ESI) m/e (M+H+) 284.2
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08163756B2 |
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| Source dataset | uspto-grants-2012_04 |
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| ORD ID | ord-fee1e28753504e98b3cbdf634a093030 |
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| Source note | uspto-grants-2012_04 |
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