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HRID 2294927作成日:2026年10月27日

Sodium Carbonate → Tert-butyl (2-(tert-butoxycarbonylaminomethyl)anilino)piperidine carboxylate

https://huagongshe.com/reaction/2294927

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium CarbonateHCID 10340—
反応物tert-Butyl 4-oxopiperidine-1-carboxylateHCID 735900—
反応物tert-butyl N-[(2-aminophenyl)methyl]carbamateHCID 4409487—
反応物Sodium triacetoxyborohydrideHCID 5049666—
溶媒1,2-DichloroethaneHCID 11—
溶媒Acetic AcidHCID 176—
溶媒ChloroformHCID 6212—
生成物Tert-butyl (2-(tert-butoxycarbonylaminomethyl)anilino)piperidine carboxylateHCID 54015391106.4%

反応手順

A mixture of 15.5 g of 2-(tert-butoxycarbonylaminomethyl)aniline, 15 g of N-t-butyloxycarbonyl-4-piperidone, 250 mL of 1,2-dichloroethane, 4.2 mL of glacial acetic acid and 25 g of sodium triacetoxyborohydride was stirred at room temperature for 48 h. The reaction mixture was poured into 500 mL chloroform and 500 mL saturated aqueous Na2CO3 and the layers separated. The aqueous layer was extracted with 2×250 mL of chloroform and the combined organic layers dried over MgSO4 and concentrated under reduced pressure. Drying overnight under vacuum gave 30.1 g of tert-butyl (2-(tert-butoxycarbonylaminomethyl)anilino)piperidine carboxylate as a solid: 1H NMR (400 MHz, CDCl3) 7.19 (t, 1H), 7.0 (d, 1H), 6.6 (dd, 2H), 4.94 (br s, 1H), 4.75 (br s, 1H), 4.23 (br m, 2H), 4.0 (br m, 2H), 3.45 (br m, 1H), 3.0 (br m, 2H), 2.0 (br m, 2H), 1.82 (br m, 1H), 1.46 (s, 9H), 1.44 (s, 9H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05691323
出典データセットuspto-grants-1997_11
ORD IDord-4aad9fe7b0b14412bd4f2c4209e19d89
出典メモuspto-grants-1997_11