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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2367108Generated: November 2, 2026

Methyl [[(methoxycarbonyl)amino](methylthio)methylene]carbamate → HCID 178502026, compound

https://huagongshe.com/reaction/2367108

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl [[(methoxycarbonyl)amino](methylthio)methylene]carbamateHCID 98708—
ReactantBenzyl 2-(3,4-diaminobenzoyl)benzoateHCID 67044774—
SolventAcetic AcidHCID 176—
ProductHCID 178502026HCID 178502026—

Reaction Steps

A solution of benzyl 2-(3,4-diaminobenzoyl)benzoate (25 g, 72 mmole) and 1,3-bis(methoxy carbonyl)-2-methyl-2-thiopseudourea (19.3 g, 94 mmole) in acetic acid (100 ml) was heated to 75° C. for 45 minutes. The solution was cooled to room temperature and concentrated in-vacuo. The resultant oil was diluted in ethyl acetate (300 mL) and washed with 1N sodium hydroxide (200 mL), water (2×200 mL), dried over sodium sulfate, filtered and concentrated in-vacuo. The resultant solid was re-crystallized using ethyl ether and ethyl acetate (2:1). The solid was isolated by vacuum filtration and washed ethyl ether to afford [5-(2-benzylcarbanoyl-benzoyl)-1H-benzoimidazol-2-yl]-carbamic acid methyl ester, 21.4 g, 49.8 mmol, (69%) as a yellow solid. 1H NMR (400 MHz, d6-DMSO): 8.04 (br s, 1H), 7.77-7.68 (m, 3H), 7.52-7.41 (m, 3H), 7.28-7.10 (m, 5H), 5.05 (s, 2H), 3.76 (s, 3H); MS (EI) for C—24H20N4O4: 430 (MH+)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08697737B2
Source datasetuspto-grants-2014_04
ORD IDord-4b078ca38a22437b9c1290038875751e
Source noteuspto-grants-2014_04