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HRID 552242作成日:2026年10月26日

Glyoxylic Acid → [(S)-5-(6-Chloro-9H-beta-carbolin-8-ylcarbamoyl)-2,2-dimethyl-morpholin-4-yl]-acetic acid

https://huagongshe.com/reaction/552242

反応式

関与物質

役割名称HCID仕込み量
反応物Glyoxylic AcidHCID 760—
反応物TriethylamineHCID 8471—
反応物Sodium cyanoborohydrideHCID 5003444—
反応物(S)-6,6-Dimethyl-morpholine-3-carboxylic acid (6-chloro-9H-beta-carbolin-8-yl)-amideHCID 67165625—
溶媒MethanolHCID 887—
溶媒WaterHCID 962—
生成物[(S)-5-(6-Chloro-9H-beta-carbolin-8-ylcarbamoyl)-2,2-dimethyl-morpholin-4-yl]-acetic acidHCID 1138451272%

反応手順

To a suspension of (S)-6,6-Dimethyl-morpholine-3-carboxylic acid (6-chloro-9H-beta-carbolin-8-yl)-amide (2.6 g, 6.0 mmoles) in 60 ml of methanol was added 1.7 ml of triethylamine (2.0 eq.), sodium cyanoborohydride (575 mg, 9.1 mmoles) and glyoxylic acid (780 mg, 8.5 mmoles). The reaction mixture was stirred at ambient temperature for 1.5 hrs. Water was added (5 ml) and the mixture was concentrated to a thick yellow slurry. More water was then added (30 ml) and the resulting slurry was stirred at ambient temperature for 10 min. and was filtered. The collected yellow solid was washed with water and dried under high vacuum to give 1.80 g (71%) of the desired product. 1H-NMR (300 MHz, DMSO-d6): δ 1.17 (s,3H), 1.30 (s,3H), 2.81 (d,1H), 3.34 (d,1H), 3.46 (d,1H), 3.56 (dd,1H), 3.84-3.90 (m,2H), 7.92 (s,1H), 8.15 (d,1H), 8.21 (s,1H), 8.36 (d,1H), 9.01 (s,1H), 10.28 (s,1H), 11.40 (s,1H). Retention Time (LC, method: ammonium acetate standard): 1.26 min. MS (M+H+): 417.1.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07951801B2
出典データセットuspto-grants-2011_05
ORD IDord-aedccd21893449fe8823a3b0b5a68fd8
出典メモuspto-grants-2011_05