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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 848150Generated: October 31, 2026

Sodium Bicarbonate → Urea, N-(5-(2-fluorophenyl)-2,3-dihydro-1-methyl-2-oxo-1H-1,4-benzodiazepin-7-yl)-N(sup 1)-(2-hydroxyethyl)-

https://huagongshe.com/reaction/848150

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
ReactantSodium MethoxideHCID 10942334—
ReactantHCID 20562331HCID 20562331—
CatalystAcetic AcidHCID 176—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
ProductUrea, N-(5-(2-fluorophenyl)-2,3-dihydro-1-methyl-2-oxo-1H-1,4-benzodiazepin-7-yl)-N(sup 1)-(2-hydroxyethyl)-HCID 3058284—

Reaction Steps

20 mg (0.048 mM) of 2-[3-[5-(o-fluorophenyl)-2,3-dihydro-1-methyl-2-oxo-1H-1,4-benzodiazepin-7-yl]ureido]ethyl acetate are dissolved in 2 ml of absolute methanol and stirred at 30°-40° C. for 1 hour with 13 mg of sodium methylate. The mixture is then buffered with a few drops of glacial acetic acid, diluted with methylene chloride, treated with 10% sodium bicarbonate solution and extracted several times with methylene chloride. The organic phases are combined, dried over sodium sulphate, filtered and concentrated. The residue is crystallised from acetone/ether. There is obtained 1-[5-(o-fluorophenyl)-2,3-dihydro-1-methyl-2-oxo-1H-1,4-benzodiazepin-7-yl]-3-(2-hydroxyethyl)urea which, according to the IR spectrum, is identical with a sample of this substance prepared in another manner (see Example 7).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04294758
Source datasetuspto-grants-1981_10
ORD IDord-d7da8517db6e46b8b50534b6b701c38e
Source noteuspto-grants-1981_10