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HRID 1173004作成日:2026年10月26日

Water → HCID 11371354、化合物

https://huagongshe.com/reaction/1173004

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物4-Pyridin-2-ylbenzaldehydeHCID 1515240—
反応物Sodium triacetoxyborohydrideHCID 5049666—
反応物(1R,2R)-2-(4-aminophenyl)cyclopropane-1-carboxylic acidHCID 68668314—
溶媒DichloromethaneHCID 6344—
溶媒1,1-DichloroethaneHCID 6365—
生成物HCID 11371354HCID 1137135422.3%

反応手順

A suspension of racemic-(trans)-2-(4-aminophenyl)cyclopropanecarboxylic acid (I-1) (0.30 g, 1.69 mmol) and 4-(2-pyridinyl)benzaldehyde (0.37 g, 2.03 mmol) in dichloroethane (10 mL) were heated to reflux until a clear solution formed. The solution was cooled to RT then NaB(OAc)3H (0.54 g, 2.54 mmol) was added and stirred for 2 h. Water (50 mL) and dichloromethane (50 mL) were added and the organic layer was separated, dried over Na2SO4, filtered and concentrated. The crude material was purified on silica gel eluting with an increasing gradient from 20% ethyl acetate/hexanes to 100% ethyl acetate to give the title compound as a white solid (0.13 g, 22%). 1H NMR (400 MHz, DMSO) δ 12.15 (s, 1H), 8.65 (d, J=4.1 Hz, 1H), 8.02 (d, J=8.3 Hz, 2H), 7.92 (d, J=8.2 Hz, 1H), 7.86 (t, J=8.0 Hz, 1H), 7.44 (d, J=8.1 Hz, 2H), 7.32 (dd, J=5.2, 6.6 Hz, 1H), 6.84 (d, J=8.4 Hz, 2H), 6.50 (d, J=8.4 Hz, 2H), 6.23 (s, 1H), 4.30 (d, J=4.6 Hz, 2H), 2.22-2.17 (m, 1H), 1.61-1.57 (m, 1H), 1.31-1.27 (m, 1H), 1.20-1.16 (m, 1H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07834013B2
出典データセットuspto-grants-2010_11
ORD IDord-275249f37c294cbe8130317dc07d1488
出典メモuspto-grants-2010_11