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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 552242생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/552242

반응식

참여 물질

역할이름HCID투입량
반응물Glyoxylic AcidHCID 760—
반응물TriethylamineHCID 8471—
반응물Sodium cyanoborohydrideHCID 5003444—
반응물(S)-6,6-Dimethyl-morpholine-3-carboxylic acid (6-chloro-9H-beta-carbolin-8-yl)-amideHCID 67165625—
용매MethanolHCID 887—
용매WaterHCID 962—
생성물[(S)-5-(6-Chloro-9H-beta-carbolin-8-ylcarbamoyl)-2,2-dimethyl-morpholin-4-yl]-acetic acidHCID 1138451272%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07951801B2
출처 데이터셋uspto-grants-2011_05
ORD IDord-aedccd21893449fe8823a3b0b5a68fd8
출처 메모uspto-grants-2011_05