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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1433061Generated: November 4, 2026

Diisopropylethylamine → HCID 69028744, compound

https://huagongshe.com/reaction/1433061

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantO-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 2733207—
Reactant3-(3-Cyanophenyl)-2-propenoic acidHCID 44725869—
ReactantHCID 53870984HCID 53870984—
SolventDimethylformamideHCID 6228—
ProductHCID 69028744HCID 69028744—

Reaction Steps

To a solution of 1-(4-amino-quinazoline-7-ylmethyl)-3-(S)-methoxymethyl-piperazine-2-one, EXAMPLE 75, (50 mg, 0.16 mmol) and 3-cyanocinnamic acid (29 mg, 0.17 mmol, prepared from 3-cyanobenzaldehyde) in 1 mL of DMF is added N,N-diisopropylethylamine (0.07 mL, 0.38 mmol), followed by 2-(1H-benzotriazol-1-yl)-1,1,3,3-tetramethyluronium tetrafluoroborate (TBTU) (59 mg, 0.18 mmol). The resulting mixture is stirred at room temperature for 16 h and the solution is concentrated. The crude product is purified by RP-HPLC eluting in a gradient of 10% CH3CN/H2O (0.1% TFA) to 60% CH3CN/H2O (0.1% TFA) over 30 min and the appropriate product fractions are combined and lyopholized to provide the title compound (73 mg, 0.13 mmol) as a white solid. 1H NMR (d6-DMSO, 300 MHz) δ9.72 (bs, 2H), 8.78 (s, 1H), 8.40 (s, 1H), 8.35 (d, 1H), 8.04 (m, 1H), 7.83 (d, 1H), 7.60 (m, 4H), 7.46 (d, 1H), 5.25-4.44 (m, 4H, rotamers), 4.02 (m, 1H), 3.66 (m, 1H), 3.51-3.40 (m, 3H), 3.27 (s, 3H). ISP MS, [M+H]+=457.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07612075B2
Source datasetuspto-grants-2009_11
ORD IDord-3dd0b3b197184c7b9ce3098cf4c78a28
Source noteuspto-grants-2009_11