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HRID 130754作成日:2026年10月26日

1-Benzylpiperazine → HCID 59730209、化合物

https://huagongshe.com/reaction/130754

反応式

関与物質

役割名称HCID仕込み量
反応物1-BenzylpiperazineHCID 75994—
反応物Sodium borohydrideHCID 4311764—
反応物6-(4-Formylphenoxy)pyridine-3-carboxamideHCID 56851422—
溶媒MethanolHCID 887—
生成物HCID 59730209HCID 5973020957%

反応手順

Combine 6-(4-formyl-phenoxy)-nicotinamide (from step 1 above) (0.300 g, 1.24 mmol) and 1-benzylpiperazine (0.35 mL, 2.01 mmol) in methanol (12 mL) and stir at ambient temperature. After 15 h, add sodium borohydride (0.108 g, 2.85 mmol) and stir. After 1 h, filter the white precipitate and dry under vacuum to give 0.283 g (57%) of the title compound as a white solid: high resolution mass spectrum (electrospray): m/z calc for C24H27N4O2 403.2134, found 403.2128: 1H NMR (DMSO-d6): 8.63 (d, 1H, J=1.5 Hz), 8.27 (dd, 1H, J=2.4, 8.3 Hz), 8.05 (s br, 1H) 7.50 (s br, 1H), 7.39-7.23 (m, 7H), 7.15-7.06 (m, 3H), 3.48 (m, 4H), 2.41 (s br, 8H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07381719B2
出典データセットuspto-grants-2008_06
ORD IDord-d4a96cb56b164a199840bc6b0ed5726a
出典メモuspto-grants-2008_06