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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1753945Generated: October 28, 2026

HCID 66679731, compound → HCID 66679067, compound

https://huagongshe.com/reaction/1753945

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 66679731HCID 66679731—
SolventMethanolHCID 887—
ProductHCID 66679067HCID 6667906798.8%

Reaction Steps

To a solution of 9-(2-benzyloxy-ethyl)-6-fluoro-2,3,4,9-tetrahydro-1H-carbazole-4-carboxylic acid diethylamide (36) (600 mg, 1.4 mmol) in methanol (40 mL) was added a slurry of Pd/C_(100 mg) in methanol (5 mL). The mixture was placed on the Parr hydrogenator and shaken for 24 h under a hydrogen atmosphere. The reaction was filtered through a pad of celite, washed with methanol and concentrated in vacuo to afford 460 mg (80%) of 6-fluoro-9-(2-hydroxy-ethyl)-2,3,4,9-tetrahydro-1H-carbazole-4-carboxylic acid diethylamide (37) as a yellow oil which was used in the next step without purification. The structure was confirmed by 1H NMR (300 MHz, MeOD-d3) δH 1.18 (3H, t, J=9 Hz, N(CH2CH3)2), 1.35 (3H, t, J=9 Hz, N(CH2CH3)2), 1.80-2.20 (4H, m, 2- and 3-CH2), 2.69-3.88 (2H, m, 1-CH2), 3.40-3.86 (6H, m, N(CH2CH3)2 and NCH2CH2OH), 4.03-4.22 (3H, m, NCH2CH2OH and 4-CH), 6.75-6.95 (2H, m, NCCHCHCFCH), and 7.05-7.15 (1H, m, NCCHCHCFCH.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09168317B2
Source datasetuspto-grants-2015_10
ORD IDord-894d741eae6948398c149b1e58ef3600
Source noteuspto-grants-2015_10