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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2276862Generated: November 2, 2026

Ammonia → HCID 90088631, compound

https://huagongshe.com/reaction/2276862

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantMethanolHCID 887—
ReactantTetrahydrofuranHCID 8028—
ReactantOxalyl chlorideHCID 65578—
ReactantHCID 18628958HCID 18628958—
ReactantHCID 90072119HCID 90072119—
CatalystDimethylformamideHCID 6228—
SolventDiethyl EtherHCID 3283—
SolventHexaneHCID 8058—
ProductHCID 90088631HCID 9008863141.7%

Reaction Steps

In a 1 L round-bottomed flask, a solution of 2-(1H-benzo[d][1,2,3]triazol-1-yl)-2-((phenoxycarbonyl)amino)acetic acid (19.37 g, 62.0 mmol) in THF (135 mL) was cooled in ice/water bath and treated with oxalyl chloride (5.43 mL, 62.0 mmol) and 4 drops DMF (bubbling). The reaction mixture was stirred for 4 hours (until HPLC analysis showed complete conversion to acid chloride). Then a solution of (2-amino-3-methylphenyl)(3-fluorophenyl)methanone (7.11 g, 31.0 mmol) in THF (35 mL) was added with 5 mL THF rinse and the resulting solution was removed from ice/water bath and stirred at room temperature for 1.5 hours. The mixture was then treated with a solution of ammonia, 7M in MeOH (19.94 mL, 140 mmol) (slight exotherm, immediately a white precipitate formed and mixture was cooled in ice/water bath). After 15 mins another portion of ammonia, 7M in MeOH (19.94 mL, 140 mmol) was added and the resulting mixture was removed from ice/water bath and sealed under N2 and stirred overnight at room temperature. The reaction mixture was concentrated to ˜½ volume and the resulting mixture was diluted with AcOH (63 mL) and stir at room temperature for 4 hours (until HPLC analysis showed complete conversion). The reaction mixture was concentrated and the residue dilute with 500 mL water and to give an orange sticky precipitate. Hexane and Et2O was added and stir at room temperature for 1 hour to form an orange solid. Et2O was removed under a stream of nitrogen and the aqueous layer was decanted. The orange sticky residue was triturate with 40 mL iPrOH and stir at room temperature to give a white precipitate. The solid was filtered and washed with iPrOH, dried on filter frit under a stream of nitrogen to give benzyl (5-(3-fluorophenyl)-9-methyl-2-oxo-2,3-dihydro-1H-benzo[e][1,4]diazepin-3-yl)carbamate (5.4 g, 41.7% yield). MS(ES):m/z=418.3 [M+H+]; HPLC: RT=3.075 min Purity=99%. (H2O/MeOH with TFA, CHROMOLITH® ODS S5 4.6×50 mm, gradient=4 min, wavelength=220 nm).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09133139B2
Source datasetuspto-grants-2015_09
ORD IDord-c24886764d724a69b0fb6c2580098a60
Source noteuspto-grants-2015_09