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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 346789생성일: 2026년 10월 25일

Hydrochloric Acid → HCID 10253417, 화합물

https://huagongshe.com/reaction/346789

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Indole-3-Butyric AcidHCID 8617—
반응물4-(4,6-Dimethoxy-1,3,5-triazin-2-yl)-4-methylmorpholinium chlorideHCID 2734059—
반응물(4-Aminomethyl-1-phenylcyclohexyl)dimethylamineHCID 21082146—
용매MethanolHCID 887—
용매2-Butanone ethanolHCID 22558530—
생성물HCID 10253417HCID 10253417—
생성물N-(4-dimethylamino-4-phenylcyclohexylmethyl)-2-(1H-indol-3-yl)butyramideHCID 21082149—

반응 단계

4-(1H-Indol-3-yl)butyric acid (232 mg, 1.0 mmol.), the mixture of the diastereoisomers of (4-aminomethyl-1-phenylcyclohexyl)dimethylamine (203 mg, 1.0 mmol.) and 4-(4,6-dimethoxy-1,3,5-triazin-2-yl)-4-methylmorpholinium chloride (415 mg, 1.5 mmol.) were dissolved in abs. methanol and stirred for 20 h at RT. For working up, the mixture was concentrated and the residue was taken up in water (15 ml), adjusted to pH 11 with 5M NaOH and extracted with EE (4×20 ml). The organic phase was washed with 1M NaOH (3 ml), dried, filtered and concentrated. The residue was a mixture of the bases of the diastereoisomeric target products, which were separated by flash chromatography on silica gel (45 g) (eluant: 700 ml methanol/EE 3:1). The non-polar diastereoisomer was obtained in a yield of 163 mg (0.39 mmol.) and was dissolved in 2-butanone/ethanol (7 ml/2 ml); isopropanolic 5M HCl (125 μl, 0.62 mmol.) was added and stirring was carried out for 2 h at RT. Concentration and drying in vacuo yielded the hydrochloride of the non-polar diastereoisomer of N-(4-dimethylamino-4-phenylcyclohexylmethyl)-2-(1H-indol-3-yl)butyramide in the form of a slightly hygroscopic white solid (177 mg, m.p. 95–100° C.).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07173045B2
출처 데이터셋uspto-grants-2007_02
ORD IDord-a546b773c4bb4beebee5ed137649b1a7
출처 메모uspto-grants-2007_02