HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 394124Generated: October 29, 2026
HCID 22648102, compound → HCID 22648062, compound
https://huagongshe.com/reaction/394124
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 22648102 | HCID 22648102 | — |
| Reactant | HCID 178418573 | HCID 178418573 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 22648062 | HCID 22648062 | — |
Reaction Steps
To a solution of methylmagnesium bromide (68 μL, 1.4M) in CH2Cl2 (0.2 mL) at 0° C. was added tert-butyl 4-{2-[5-(2-chlorophenyl)-1-(2,6-dichlorophenyl)-3-(4-methoxybenzyl)-2-oxo-1,2,3,4-tetrahydroquinazolin-7-yl]-2-oxoethyl}piperazine-1-carboxylate (EXAMPLE ABA4, Step A) (35.6 mg, 0.047 mmol) dissolved in CH2Cl2 (0.3 mL) slowly. The reaction mixture was stirred for 2 h while warming up to rt. It was quenched with saturated aqueous solution of NH4Cl, and extracted with CH2Cl2. The combined organic layers were washed with brine and dried over Na2SO4. After removal of the solvent, the crude product was purified by preparative thin layer chromatography eluting with 1:3 acetone:hexane to obtain the title compound. Mass spectrum (ESI): 765.2 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06809199B2 |
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| Source dataset | uspto-grants-2004_10 |
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| ORD ID | ord-c8d1104dbbb647cc895b434dad5b3c07 |
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| Source note | uspto-grants-2004_10 |
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