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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1509728Generated: October 30, 2026

Diisopropylethylamine → HCID 178495690, compound

https://huagongshe.com/reaction/1509728

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
Reactant(2S)-2-((methoxycarbonyl)amino)-3-methylbutanoic acidHCID 10942966—
ReactantHCID 178495707HCID 178495707—
SolventDimethylformamideHCID 6228—
ProductHCID 178495690HCID 178495690—

Reaction Steps

A mixture of methyl {(1R)-2-[(2S)-2-(9-{2-[(2S,4S)-4-(methoxymethyl)pyrrolidin-2-yl]-1H-imidazol-5-yl}-1,11-dihydroisochromeno[4′,3′:6,7]naphtho[1,2-d]imidazol-2-yl)pyrrolidin-1-yl]-2-oxo-1-phenylethyl}carbamate (55 mg, 0.077 mmol), (S)-2-(methoxycarbonylamino)-3-methylbutanoic acid (14 mg, 0.077 mmol), HATU (32 mg, 0.085 mmol) and 0.4 mL 10% DIPEA in DMF was stirred at room temperature for 1 hour. The product was purified by reverse phase HPLC. The product was converted to the free base by dissolution in 2 mL 1:1 acetonitrile:methanol and passage through a prepacked cartridge of polymer supported carbonate. The eluent was concentrated, the taken up in 1% TFA in 1:1 acetonitrile:water, frozen, and lyophilized to give the product as a trifluoroacetate salt. (30.7 mg)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09221833B2
Source datasetuspto-grants-2015_12
ORD IDord-9e2b0e4166fa4b0fbf04fb78a3555a4c
Source noteuspto-grants-2015_12