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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1256361Generated: October 31, 2026

Trifluoroacetic acid → HCID 131730619, compound

https://huagongshe.com/reaction/1256361

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 67064824HCID 67064824—
SolventDichloromethaneHCID 6344—
ProductHCID 131730619HCID 13173061941%

Reaction Steps

tert-Butyl 7-(5-(4-(2-hydroxypropan-2-yl)benzamido)pyrazolo[1,5-a]pyrimidin-7-yl)-3,4-dihydroisoquinoline-2(1H)-carboxylate from Step A was dissolved in CH2Cl2 (2 ml). Trifluoroacetic acid (2 ml) was then added at 0° C. The mixture was stirred for 30 minutes at that temperature before being concentrated in vacuo. Residual trifluoroacetic acid was removed azeotropically with toluene twice. The residue was then dissolved in acetonitrile before being purified by preparatory HPLC (20-30% MeCN/H2O gradient+0.01% TFA) to give the titled compound as a white powder (50 mg, 41% yield). 1H NMR (400 MHz, DMSO-d6) δ=11.30 (s, 1 H), 9.14 (br. s., 2 H), 8.21 (d, J=2.5 Hz, 1 H), 8.07 (s, 1 H), 8.05-8.01 (m, 2 H), 8.00-7.95 (m, 1 H), 7.65-7.60 (m, 2 H), 7.50 (d, J=8.1 Hz, 1 H), 6.60 (d, J=2.3 Hz, 1 H), 4.47-4.40 (m, 2 H), 3.47 (br. s., 2 H), 3.13 (t, J=6.2 Hz, 2 H), 1.46 (s, 6 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08461163B2
Source datasetuspto-grants-2013_06
ORD IDord-554bddc898ab4f8582504217c23d66c3
Source noteuspto-grants-2013_06