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HRID 615570作成日:2026年10月26日

Hydrochloric Acid → tert-butyl N-{3-[(3-aminopropyl)(methyl)amino]propyl}carbamate

https://huagongshe.com/reaction/615570

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物WaterHCID 962—
反応物N,N-bis(3-aminopropyl)methylamineHCID 7777—
反応物O-(1,1-Dimethylethyl) S-(4,6-dimethyl-2-pyrimidinyl) carbonothioateHCID 148428—
溶媒TriethylamineHCID 8471—
溶媒1,4-DioxaneHCID 31275—
生成物tert-butyl N-{3-[(3-aminopropyl)(methyl)amino]propyl}carbamateHCID 1298366070.8%

反応手順

Into 180 ml of water, was dissolved 150 g of bis(3-aminopropyl)methylamine followed by 53 g of triethylamine. To the solution, while being cooled in ice and stirred, was added portionwise a solution of 83 g (1/3 equivalent) of 4,6-dimethyl-2-tert-butoxycarbonylthiopyrimidine in 200 ml of dioxane. The mixture was allowed to react at room temperature for 5 hours. The reaction mixture was stripped of the dioxane and triethyl amine by disillation under reduced pressure. The residue was adjusted to pH 2 with 6N hydrochloric acid and washed with chloroform. The aquoues layer was adjusted to pH 13.5 with sodium hydroxide and extracted with chloroform. The chloroform layer was dried over sodium sulfate and freed from the solvent by distillation under reduced pressure to yield 60 g (24% yield) of (3-tert-butoxycarbonylaminopropyl)-(3-aminopropyl)methylamine (BOC-APMP).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04500452
出典データセットuspto-grants-1985_02
ORD IDord-d4222fa452ae4fcd82b9c1b4812f7090
出典メモuspto-grants-1985_02