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HRID 251082作成日:2026年10月26日

tert-butyl N-(4-aminobutyl)carbamate → {4-[(1-methyl-1H-benzoimidazol-2-ylmethyl)-amino]-butyl}-carbamic acid tert-butyl ester

https://huagongshe.com/reaction/251082

反応式

関与物質

役割名称HCID仕込み量
反応物tert-butyl N-(4-aminobutyl)carbamateHCID 4351—
反応物1-methyl-1H-1,3-benzodiazole-2-carbaldehydeHCID 762084—
反応物Sodium triacetoxyborohydrideHCID 5049666—
溶媒DichloromethaneHCID 6344—
生成物{4-[(1-methyl-1H-benzoimidazol-2-ylmethyl)-amino]-butyl}-carbamic acid tert-butyl esterHCID 67272476—

反応手順

Using General Procedure B, reaction of 1-methyl-1H-benzoimidazole-2-carbaldehyde and (4-amino-butyl)-carbamic acid tert-butyl ester in CH2Cl2 with NaBH(OAc)3 gave {4-[(1-methyl-1H-benzoimidazol-2-ylmethyl)-amino]-butyl}-carbamic acid tert-butyl ester as a sticky white foam. 1H NMR (CDCl3) δ 1.43 (s, 9H), 1.54-1.64 (m, 4H), 1.80-1.82 (m, 2H), 2.67-2.75 (m, 2H), 3.12-3.13 (m, 2H), 3.82 (s, 3H), 4.06 (s, 2H), 7.23-7.30 (m, 2H), 7.31-7.38 (m, 1H), 7.70-7.76 (m, 1H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07863293B2
出典データセットuspto-grants-2011_01
ORD IDord-2d402fb1aae84987912e9acc2d2dd017
出典メモuspto-grants-2011_01