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HRID 1056076作成日:2026年10月27日

Aniline → 8-bromo-N-phenylquinazolin-2-amine

https://huagongshe.com/reaction/1056076

反応式

関与物質

役割名称HCID仕込み量
反応物AnilineHCID 6115—
反応物Ammonium ChlorideHCID 25517—
反応物Lithium HexamethyldisilazideHCID 2733832—
反応物8-Bromo-2-chloroquinazolineHCID 45790061—
溶媒TetrahydrofuranHCID 8028—
生成物8-bromo-N-phenylquinazolin-2-amineHCID 89781929100%

反応条件

温度0 °C

反応手順

LHMDS (1.0M in THF; 4.11 mL, 4.11 mmol) was added to a solution of 8-bromo-2-chloroquinazoline (Ark Pharm, Inc., Libertyville, Ill.; 500 mg, 2.053 mmol) and aniline (0.337 mL, 3.70 mmol) in THF (10 mL) at 0° C., and the resulting solution was stirred at 0° C. for 10 min. Saturated aq. NH4Cl (10 mL) was added, and the resulting mixture was partitioned between EtOAc (50 mL) and additional saturated aq. NH4Cl (30 mL). The organic layer was separated, washed with brine (30 mL), dried over Na2SO4, filtered and concentrated in vacuo. Chromatographic purification of the residue (silica gel, 0-10% MeOH/DCM) furnished 8-bromo-N-phenylquinazolin-2-amine (616 mg, 2.052 mmol, 100% yield) as a yellow solid: m/z (ESI, +ve) 300.0 (M+H)+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09394297B2
出典データセットuspto-grants-2016_07
ORD IDord-186b83400f264668b58b6ad833df54ab
出典メモuspto-grants-2016_07