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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 49723Generated: October 31, 2026

Diisopropylethylamine → HCID 17946656, compound

https://huagongshe.com/reaction/49723

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(3-Acetoxy-4-nitro-phenyl)acetic acidHCID 17946639—
Reactantethyl (3RS)-3-(5-aminopyrid-2-yl)butyrateHCID 17946645—
SolventDimethylformamideHCID 6228—
ProductHCID 17946656HCID 17946656—

Reaction Conditions

Temperature30 °C

Reaction Steps

A solution of O-(7-azabenzotriazol-1-yl)-1,1,3,3-tetramethyluronium hexafluorophosphate (10.95 g) in dry dimethylformamide (20 mL) was added to a solution of (RS) ethyl 3-(5-aminopyrid-2-yl)butanoate (3.0 g, Reference Example 5), diisopropylethylamine (10 mL) and (3-acetoxy-4-nitro-phenyl)acetic acid (6.89 g, Reference Example 17) in dimethylformamide (90 mL) under a nitrogen atmosphere. After stirring at 30° C. for 24 hours the reaction mixture was evaporated and the residue was partitioned between ethyl acetate and 5% aqueous sodium bicarbonate. The organic phase was washed with water, then with brine, then dried over magnesium sulphate, then treated with decolourising charcoal followed by filtration and evaporation of the filtrate to give the title compound as a dark oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06706738B2
Source datasetuspto-grants-2004_03
ORD IDord-9ba64a1116f449bb9ec1ca7dc4da51be
Source noteuspto-grants-2004_03