Triethylamine → HCID 178489169、化合物
反応式
[CH3:1][O:2][C:3]1[CH:10]=[CH:9][C:6]([C:7]#[N:8])=[CH:5][C:4]=1[N+:11]([O-])=O.[N-:14]=[N+:15]=[N-:16].[Na+].C(N(CC)CC)C.[H][H]>C1(C)C=CC=CC=1.CO.[Pd].O>[CH3:1][O:2][C:3]1[CH:10]=[CH:9][C:6]([C:7]2[NH:16][N:15]=[N:14][N:8]=2)=[CH:5][C:4]=1[NH2:11]参加物
反応条件
- 温度
- 100 °C
実験手順
To a solution of 4-methoxy-3-nitro-benzonitrile (2.5 g, 1.4 mmol) in toluene (20 ml) was added sodium azide (1.3 g, 1.8 mmol) and triethylamine hydrochlride (1.5 g, 1.8 mmol), and this mixture stirred at 100° C. fro 48 h. Water was then added (200 ml) and the mixture agitated, the aqueous phase was further washed with water (2×30 ml). The organic phase was then adjusted to pH 2 and the solid which precipitated was filtered off and washed further with water (100 ml) then dried in vacuo (0.05 mmHg, 60° C.) to afford the crude tetrazole. This material was then directly dissolved in MeOH (80 ml), Pd/C (10%) (250 mg) was added and the mixture stirred under 1 atm of hydrogen at 20° C. for ca. 1 h until the theoretical amount of hydrogen (ca. 880 ml) had been taken up. The catalyst was then filtered off and the solvent evaporated to afford the title compound as a white solid (2.2 g, 82% yield), MS: m/e=191.1 (M+).
後処理
- stirringthe mixture agitated
- washthe aqueous phase was further washed with water (2×30 ml)
- customthe solid which precipitated
- filtrationwas filtered off
- washwashed further with water (100 ml)
- customthen dried in vacuo (0.05 mmHg, 60° C.)
- customto afford the crude tetrazole
- filtrationThe catalyst was then filtered off
- customthe solvent evaporated
出典と根拠
- ORDレコード
- ord-3deb7daaa97c440baea705f147399f22
- 出典データセット
- uspto-grants-2005_11
- 特許番号
- US06963000B2
反応ノート
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