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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1793123Generated: November 3, 2026

HCID 11046685, compound → HCID 11113481, compound

https://huagongshe.com/reaction/1793123

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 11046685HCID 11046685—
SolventMethanolHCID 887—
ProductHCID 11113481HCID 1111348146.2%

Reaction Steps

Iodide 6d (0.45 g; 1.1 mmol) was used as starting material. After cooling to rt, the reaction mixture was diluted with CH3OH and filtered. The filtrate was evaporated under vacuum, and the residue was recrystallized from CH3OH to afford 0.12 g (45%) of 1d as a white solid. mp>260 C; TLC (CH2Cl2-EtOAc, 1:1): Rf=0.51; 1H NMR (CDCl3): δ 0.88 (br t, 6H), 0.97 (t, 6H), 1.31 (br m, 12H), 1.60 (m, 4H), 1.72 (m, 4H), 3.06 (t, 4H), 3.38 (q, 4H), 7.00 (br t, 2H); 13C NMR (DMSO-d6): δ 14.2, 14.6, 22.8, 23.1, 26.9, 30.2, 31.7, 38.7, 131.3, 137.2, 163.5; UV/vis (CH3OH): max (M−1cm−1)=287 (26000), 295 (25900), 309 (14100); LRMS (CI+): m/z (%): 473 (100) [M+H]+; HRMS (CI+): calcd for C26H45N6O2 473.3604; found 473.3601; Anal. calcd for C26H44N6O2: C, 66.07; H, 9.38; N, 17.78; found: C, 66.26; H, 9.54; N, 17.83.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07078528B2
Source datasetuspto-grants-2006_07
ORD IDord-d2419e508c674da0968fc6df07f52955
Source noteuspto-grants-2006_07