반응 #1973915

ord-a787ea647cc7495b94cc88e3d1582b78

반응 방정식

COc1cccc2c1c1c(n2CCF)CCCC1C(=O)O
9-(2-Fluoroethyl)-5-methoxy-2,3,4,9-tetrahydro-1H-carbazole-4-carboxylic acid
O=C(Cl)C(=O)Cl
Oxalyl chloride
CN(C)C=O
DMF
COc1cccc2c1c1c(n2CCF)CCCC1C(=O)Cl
9-(2-fluoroethyl)-5-methoxy-2,3,4,9-tetrahydro-1H-carbazole-4-carbonyl chloride
수율 99.8%

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타then evaporated in vacuo

실험 절차

A solution of 9-(2-Fluoroethyl)-5-methoxy-2,3,4,9-tetrahydro-1H-carbazole-4-carboxylic acid (17) (347 mg, 1.2 mmol) in dry dichloromethane (2 mL) was stirred under nitrogen. Oxalyl chloride (453 mg, 3.6 mmol, 300 μL) was added followed by a drop of DMF. The reaction mixture was stirred at RT under nitrogen for 2 h then evaporated in vacuo to give 371 mg (quantitative) of 9-(2-fluoroethyl)-5-methoxy-2,3,4,9-tetrahydro-1H-carbazole-4-carbonyl chloride as a gum which was used in the next step without purification. The structure was confirmed by 13C NMR (75 MHz, CDCl3): δC 20.2, 21.7, 26.4, 43.3 (d, JCF=23 Hz), 54.9, 80.5, 83.1, 100.2, 102.2, 105.8, 116.7, 122.4, 135.5, 137.4, 153.5, and 176.6.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US08501153B2uspto-grants-2013_08