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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2040670Generated: November 2, 2026

Hydrochloric Acid → HCID 178457041, compound

https://huagongshe.com/reaction/2040670

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant7-[(3aS,4R,6R,6aR)-6-({[(3-{[6-chloro-5-(trifluoromethyl)-1-{[2-(trimethylsilyl)ethoxy]methyl}-1H-1,3-benzodiazol-2-yl]methyl}cyclobutyl)methyl](propan-2-yl)amino]methyl)-2,2-dimethyl-hexahydrocyclopenta[d][1,3]dioxol-4-yl]-7H-pyrrolo[2,3-d]pyrimidin-4-amineHCID 67776357—
SolventMethanolHCID 887—
ProductHCID 178457041HCID 17845704127%

Reaction Conditions

Temperature40 °C

Reaction Steps

12N HCl (1.5 ml) was added slowly to a solution of 7-[(3aS,4R,6R,6aR)-6-({[(3-{[6-chloro-5-(trifluoromethyl)-1-{[2-(trimethylsilyl)ethoxy]methyl}-1H-1,3-benzodiazol-2-yl]methyl}cyclobutyl)methyl](propan-2-yl)amino}methyl)-2,2-dimethyl-hexahydrocyclopenta[d][1,3]dioxol-4-yl]-7H-pyrrolo[2,3-d]pyrimidin-4-amine (174 mg, 0.22 mmol) in MeOH (1.5 ml) and stirred at 40° C. for 6 h. The reaction was monitored by LCMS, no starting material seen after 2.5 h. The reaction mixture was concentrated in vacuo, then basified with 7N NH3 in MeOH (5 ml). This was then evaporated to dryness. Purification by silica gel column chromatography, eluting with 7N NH3 in MeOH:DCM (1:9) gave the desired product (36 mg, 27%) as a white solid; MS (ESI+) for C29H35ClF3N7O2 m/z 606.30 [M+H]+; HPLC purity 100% (ret. time, 2.59 min); 1H NMR (500 MHz, MOD) δH ppm 0.93-1.09 (6 H, m), 1.41-1.64 (2 H, m), 1.76-2.06 (1 H, m), 2.15-2.65 (9 H, m), 2.65-2.88 (1 H, m), 2.91-3.13 (3 H, m), 3.80-4.09 (1 H, m), 4.19-4.46 (1 H, m), 4.88-4.94 (1 H, m), 6.46-6.77 (1 H, m), 7.19 (1 H, d, J=3.63 Hz), 7.69 (1 H, s), 7.89 (1 H, s), 8.06 (1 H, s)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08580762B2
Source datasetuspto-grants-2013_11
ORD IDord-2d3b222d65ee428b8c3acd786610cad9
Source noteuspto-grants-2013_11