Trifluoroacetic acid methylene chloride → HCID 22311992, compound

HRID 966121Notes

Reaction equation

HRID 966121 reaction equation
C(OC([N:8]1[CH2:13][CH2:12][CH:11]([C:14]2[C:18]3[CH:19]=[N:20][C:21]([N:23]4[CH2:28][CH2:27][O:26][CH2:25][CH2:24]4)=[CH:22][C:17]=3[NH:16][CH:15]=2)[CH2:10][CH2:9]1)=O)(C)(C)C.C(O)(C(F)(F)F)=O.C(Cl)Cl>>[N:23]1([C:21]2[N:20]=[CH:19][C:18]3[C:14]([CH:11]4[CH2:12][CH2:13][NH:8][CH2:9][CH2:10]4)=[CH:15][NH:16][C:17]=3[CH:22]=2)[CH2:24][CH2:25][O:26][CH2:27][CH2:28]1

Participants

3

Reactant 2

HCID 21863450Trifluoroacetic acid methylene chlorideHCID 69182577HCID 69182577, compound

Product 1

HCID 22311992HCID 22311992, compoundYield 100.1%

Procedure

4-(6-Morpholin-4-yl-1H-pyrrolo[3,2-c]pyridin-3-yl)-piperidine-1-carboxylic acid tert-butyl ester (380 mg, 0.98 mmol) was set stirring in 1:1 TFA/CH2Cl2. After 45 min the mixture was evaporated. The residue was dissolved in MeOH (20 mL) and neutralized with DOWEX 550A OH anion exchange resin to pH 8. The resin was then filtered off and MeOH was removed under reduced pressure to give 281 mg (100%) of a yellow solid. MS (electrospray): exact mass calculated for C16H22N4O, 286.18; m/z found, 287.1 [M++H].

Workup

  1. customAfter 45 min the mixture was evaporated
  2. dissolutionThe residue was dissolved in MeOH (20 mL)
  3. filtrationThe resin was then filtered off
  4. customMeOH was removed under reduced pressure

Sources & evidence

ORD record
ord-508cdfdd7d2f4039aa143cd459f3cc18
Source dataset
uspto-grants-2005_10
Patent number
US06951851B2

Reaction notes

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