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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1297516Generated: October 29, 2026

HCID 136065296, compound → HCID 136065301, compound

https://huagongshe.com/reaction/1297516

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 136065296HCID 136065296—
SolventDichloromethaneHCID 6344—
SolventTrifluoroacetic acidHCID 6422—
ProductHCID 136065301HCID 136065301—

Reaction Steps

A solution of tert-butyl 4-{N-[(6RS)-2-methoxymethyl-4-oxo-3,4,7,8-tetra-hydro-6H-cyclopenta[g]quinazolin-6-yl]-N-(prop-2-ynyl)amino}benzoate (0.069 g, 0.15 mmol) in dichloromethane (1 ml) and trifluoroacetic acid (3 ml) was stirred at room temperature for 1 hour and 10 min, then the solvents were removed in vacuo. The residue was triturated with diethyl ether and the precipitate was collected by filtration, washed with diethyl ether and dried in vacuo over P2O5 to afford the title compound as the tifluoroacetate salt: 0.061 g, m.p. 225° C. (dec); 1H-NMR (250 MHz, DMSO-d6, TMS) 2.23, 2.53 (obscured by DMSO peak) (2×m, each 1H, 7-H), 2.90-3.20 (m, 3H, C≡CH, 8-H), 3.34 (s (obscured by the H2O peak), 3H, OCH3), 3.97 (ABq, J=18.0 Hz, 2H, CH2C≡C), 4.32 (s, 2H, 2-CH2), 5.79 (t, J=8.1 Hz, 1H, 6-H), 7.03 (d, J=9.02 Hz, 2H, 3′, 5′-H), 7.58, (s, 1H, 9-H), 7.81 (m, 3H, 5-H, 2′, 6′-H), 12.17 (s, 1H, N3-H); MS (ESI, m/z) 426 {(M+Na)+, 25%}, 404 {(M+H)+, 70%}.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07250511B2
Source datasetuspto-grants-2007_07
ORD IDord-bede690f4cad46a3b271ae8457fcf254
Source noteuspto-grants-2007_07