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HRID 965196作成日:2026年10月26日

Triethylamine → 2-chloro-N-(3-iodobenzyl)-7H-purin-6-amine

https://huagongshe.com/reaction/965196

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物3-Iodobenzylamine hydrochlorideHCID 2723861—
反応物2,6-DichloropurineHCID 5324412—
溶媒EthanolHCID 702—
生成物2-chloro-N-(3-iodobenzyl)-7H-purin-6-amineHCID 1031794960%

反応手順

A solution of 2,6-dichloropurine (Aldrich Chemical Co., 1 g, 5.3 mmol), 3-iodobenzylamine hydrochloride (1.7 g, 5.8 mmol), and triethylamine (2.2 ml, 15.35 mmol) in ethanol (10 ml) was stirred for 5 days at room temperature. The colorless solid formed was collected by suction, washed with small amount of cold ethanol, and dried to yield 2-chloro-N6 -(3-iodobenzyl)adenine (1.16 g, 60%): m.p. 222°-224° C.; mass (EI) 385: 1H NMR (DMSO-d6 d 4.59 (br s, 2H, --CH2), 7.13 (pseudo t, J=8.2 and 7.5 Hz, 1H, Bn), 7.36 (d, J=7.5 Hz, 1H, Bn), 7.61 (d, J=7.5 Hz, 1H, Bn), 7.74 (s, 1H, Bn), 8.14 (s, 1H, H-8), 8.76 (br s, 1H, exchangeable with D2O, NH), 13.14 (br s, 1H, exchangeable with D2O, NH). UV (MeOH) 1max 281.7, 257.5, 232.5 nm.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05773423
出典データセットuspto-grants-1998_06
ORD IDord-a5c0adb6a8bc4171a673c244737923b7
出典メモuspto-grants-1998_06