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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 882647Generated: October 30, 2026

Triethylamine → HCID 86678410, compound

https://huagongshe.com/reaction/882647

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantBromoacetyl chlorideHCID 89602—
ReactantHCID 86678411HCID 86678411—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86678410HCID 86678410—

Reaction Conditions

Temperature0 °C

Reaction Steps

22 mg (0.023 mmol) of N-(6-aminohexyl)-N-methyl-L-valyl-N-[(3R,4S,5S)-1-{(2S)-2-[(1R,2R)-3-{[(2S)-3-(1H-indol-3-yl)-1-(1,2-oxazinan-2-yl)-1-oxopropan-2-yl]amino}-1-methoxy-2-methyl-3-oxopropyl]pyrrolidin-1-yl}-3-methoxy-5-methyl-1-oxoheptan-4-yl]-N-methyl-L-valinamide (Intermediate 101) were dissolved in 9.5 ml of THF and admixed at 0° C. with 4.2 μl of triethylamine. A solution of bromoacetyl chloride in THF was added dropwise and the reaction mixture was stirred at 0° C. for 30 min. The reaction mixture was concentrated and the residue was purified by preparative HPLC. Thus, 6.9 mg (26% of theory) of the title compound were obtained as a foam.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08992932B2
Source datasetuspto-grants-2015_03
ORD IDord-02e57c5dc84443e187eea8bb5a7edb36
Source noteuspto-grants-2015_03