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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 717738Generated: October 31, 2026

Bis(2-amino-1H-imidazole) sulphate → HCID 178453510, compound

https://huagongshe.com/reaction/717738

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBis(2-amino-1H-imidazole) sulphateHCID 135136—
ReactantSodium MethoxideHCID 10942334—
Reactant2-(4-{[tert-Butoxycarbonyl-(3-tert-butoxycarbonylamino-propyl)-amino]-methyl}-phenyl)-3-methoxy-acrylic acid methyl esterHCID 66578805—
SolventEthanolHCID 702—
ProductHCID 178453510HCID 17845351048.2%

Reaction Steps

To a mixture of 2-(4-{[tert-Butoxycarbonyl-(3-tert-butoxycarbonylamino-propyl)-amino]-methyl}-phenyl)-3-methoxy-acrylic acid methyl ester (97 mg, 0.2 mmol), 1H-imidazol-2-ylamine sulfate (29 mg, 0.223 mmol) and ethanol (10 mL) was added a solution of sodium methoxide (0.5 mL, 0.5 M in methanol, 0.25 mmol). The resulted mixture was refluxed for 18 h, additional 0.5 mL of sodium methoxide (0.5 M in methanol, 0.5 mmol) was added and continued to reflex for 20 h. The reaction was concentrated and diluted with EtOAc (30 mL) and washed with water (20 mL), brine (20 mL). The EtOAc solution was concentrated. The crude product was purified by flash chromatography (10% methanol in dichloromethane) to give desired product (48 mg, 48%) as white solid. 1NMR (300 MHz, CD3OD): δ 8.40 (s, 1H), 7.59 (br.s, 2H), 7.29 (m, 4H), 4.46 (s, 2H), 3.23 (m, 2H), 3.02 (m, 2H), 1.68 (m, 2H), 1.52 (br.d, 9H), 1. 42 (s, 9H). LCMS (EI) m/z: 498.1 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09193731B2
Source datasetuspto-grants-2015_11
ORD IDord-7994259b567445fa94a6c609771e7e26
Source noteuspto-grants-2015_11