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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1863842Generated: October 27, 2026

Water → 2,5,6-Trichloro-3-[N-(methoxycarbonylamino)iminomethylidene]-1-(beta-D-ribofuranosyl)indole

https://huagongshe.com/reaction/1863842

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantMethyl carbazateHCID 80519—
ReactantFtcriHCID 3011610—
SolventMethanolHCID 887—
Product2,5,6-Trichloro-3-[N-(methoxycarbonylamino)iminomethylidene]-1-(beta-D-ribofuranosyl)indoleHCID 8659897085%

Reaction Steps

2,5,6-Trichloro-3-formyl-1-(β-D-ribofuranosyl)indole (4.3, 122 mg, 0.32 mmol) was dissolved in MeOH (10 mL) to which was added methyl hydrazinocarboxylate (115 mg, 1.3 mmol). The resulting solution was heated on a 60 C oil bath for 16 h, then cooled to room temperature and poured into 100 mL of water, and the solvent evaporated to approx 50 mL. The resulting suspension was cooled to 4 C, then filtered and the solids rinsed with cold water (25 mL). The solids were recrystallized from boiling EtOAc/hexane to yield 123 mg (85%) of 4.31 as a pale pink crystalline solid: mp 217-219 C; Rf0.2 (10% MeOH/CHCl3); 1H-NMR (500 MHz, DMSO-d6): δ 11.17 (b, 1H, D2O exch.), 8.54 (s, 1H), 8.42 (s, 1H), 8.22 (b, 1H), 5.92 (d, 1H), 5.42-5.37 (m, 2H, D2O exch.), 5.25 (d, 1H, D2O exch.), 4.43 (q, 1H), 4.15 (d, 1H), 3.98 (d, 1H), 3.72 (b, 5H). 13C-NMR (125 MHz, DMSO-d6): δ 153.88, 133.17, 129.33, 126.08, 124.96, 124.06, 122.17, 115.34, 108.59, 88.76, 86.03, 71.30, 69.73, 69.62, 61.07, 52.04. HRMS (ES) m/z calcd. for C16H16Cl3N3O6.Na 474.0002, found 473.9999. Anal calcd for C16H16Cl3N3O6.¼H2O: C, 42.03; H, 3.64; N, 9.19. Found: C, 42.11; H, 3.92; N, 9.18.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07625871B2
Source datasetuspto-grants-2009_12
ORD IDord-f5579af5d23147ce8adc6a062faa1030
Source noteuspto-grants-2009_12