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HRID 14692作成日:2026年10月23日

Phenethylamine → 3-(1-Aminomethyl-6,8-dimethoxy-isoquinolin-4-yl)-1-benzyl-1-methyl-thiourea

https://huagongshe.com/ja/reaction/14692

反応式

関与物質

役割名称HCID仕込み量
反応物PhenethylamineHCID 1001—
反応物TriethylamineHCID 8471—
反応物ThiophosgeneHCID 10040—
反応物2-(4-Amino-6,8-dimethoxy-isoquinolin-1-ylmethyl)-isoindole-1,3-dioneHCID 59341090—
溶媒DichloromethaneHCID 6344—
生成物3-(1-Aminomethyl-6,8-dimethoxy-isoquinolin-4-yl)-1-benzyl-1-methyl-thioureaHCID 5934107239%

反応手順

Triethylamine (46 μL, 0.33 mmol) and then thiophosgene (13 μL, 0.16 mmol) were added to a solution of Example 45C (40 mg, 0.11 mol) in dichloromethane (3 mL), and the reaction stirred for 1 h at r.t. N-benzylmethylamine (46 μL, 0.33 mmol) was added, and the reaction stirred for 1 h. Solvent was removed in vacuo, and the residue was deprotected with a solution of hydrazine (0.1 mL) in ethanol (4 mL), stirring for 1 h. Purification by Prep-HPLC gave 18 mg (39%) of the title compound (TFA salt) as a yellow solid. H1-NMR (MeOD-d4): δ 8.15 (s, 1H), 7.22-7.38 (m, 5H), 6.70 (s, 1H), 6.66 (s, 1H), 5.18 (s, 2H), 4.58 (s, 2H), 3.96 (s, 3H), 3.81 (s, 3H), 3.23 (s, 3H). MS (ES) (M+H) calc'd for C21H24N4O2S, 397; found 397.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07732446B1
出典データセットuspto-grants-2010_06
ORD IDord-37fe3da4ac1f45b6b20bca988a913546
出典メモuspto-grants-2010_06