Diethyl Ether → HCID 11178018, compound

HRID 751423Notes

Reaction equation

HRID 751423 reaction equation
C(OC([N:8]1[CH2:14][CH2:13][CH2:12][N:11]([C:15]2[N:23]([C:24]3[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=3)[C:18]3=[N:19][CH:20]=[CH:21][CH:22]=[C:17]3[C:16]=2[CH:30]=[O:31])[CH2:10][CH2:9]1)=O)(C)(C)C.FC(F)(F)C(O)=O.C(#N)C.CCOCC>ClCCl>[N:11]1([C:15]2[N:23]([C:24]3[CH:25]=[CH:26][CH:27]=[CH:28][CH:29]=3)[C:18]3=[N:19][CH:20]=[CH:21][CH:22]=[C:17]3[C:16]=2[CH:30]=[O:31])[CH2:12][CH2:13][CH2:14][NH:8][CH2:9][CH2:10]1

Participants

6

Procedure

A solution of 4-(3-formyl-1-phenyl-1H-pyrrolo[2,3-b]pyridin-2-yl)-[1,4]diazepane-1-carboxylic acid tert-butyl ester (330 mg, 0.786 mmol) in dichloromethane (20 mL) is treated with trifluoroacetic acid (0.60 mL, 6.04 mmol). The resulting solution is allowed to stir at room temperature for 22 hours before treating the reaction with a further aliquot of trifluoroacetic acid (0.60 mL, 6.04 mmol). After stirring for a further 18 hours, the reaction mixture is evaporated to give a gooey red oil. Trituration of the crude product salt with acetonitrile and ether gives 285 mg of 2-[1,4]diazepan-1-yl-1-phenyl-1H-pyrrolo[2,3-b]pyridine-3-carbaldehyde; trifluoro-acetic acid salt as a pink solid (84% yield). LC/MS: retention time 2.25 min, m/e 321 (M+H). 1H NMR (300 MHz, DMSO-d6): 10.15 (1H, s), 8.60 (2H, br.s), 8.36 (1H, dd), 8.08 (1H, dd), 7.63-7.48 (5H, m), 7.22 (1H, dd), 3.63-3.48 (4H, m), 3.11-2.95 (4H, m), 1.81 (2H, m).

Workup

  1. additionbefore treating
  2. stirringAfter stirring for a further 18 hours
  3. customthe reaction mixture is evaporated
  4. customto give a gooey red oil

Sources & evidence

ORD record
ord-47cfefcb6baa47a7bcfbeef00920ef02
Source dataset
uspto-grants-2008_07
Patent number
US07405300B2

Reaction notes

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