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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Bis(2-amino-1H-imidazole) sulphate | HCID 135136 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | 2-(4-{[tert-Butoxycarbonyl-(3-tert-butoxycarbonylamino-propyl)-amino]-methyl}-phenyl)-3-methoxy-acrylic acid methyl ester | HCID 66578805 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178453510 | HCID 178453510 | 48.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09193731B2 |
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| Source dataset | uspto-grants-2015_11 |
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| ORD ID | ord-7994259b567445fa94a6c609771e7e26 |
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| Source note | uspto-grants-2015_11 |
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