Hydrochloric Acid → HCID 59447037, compound

HRID 1746798Notes

Reaction equation

HRID 1746798 reaction equation
[CH:1]1([CH2:4][N:5]([CH2:32][CH2:33][CH3:34])[C:6]2[N:11]=[CH:10][N:9]=[C:8]([C:12]([NH:14][C:15]3[CH:31]=[CH:30][C:18]([CH2:19][S:20]([CH2:23][CH2:24][C:25]([O:27]CC)=[O:26])(=[O:22])=[O:21])=[CH:17][CH:16]=3)=[O:13])[CH:7]=2)[CH2:3][CH2:2]1.Cl>C1COCC1>[CH:1]1([CH2:4][N:5]([CH2:32][CH2:33][CH3:34])[C:6]2[N:11]=[CH:10][N:9]=[C:8]([C:12]([NH:14][C:15]3[CH:31]=[CH:30][C:18]([CH2:19][S:20]([CH2:23][CH2:24][C:25]([OH:27])=[O:26])(=[O:22])=[O:21])=[CH:17][CH:16]=3)=[O:13])[CH:7]=2)[CH2:2][CH2:3]1

Participants

4

Procedure

A solution of ethyl 3-({4-[({6-[(cyclopropylmethyl)(propyl)amino]pyrimidin-4-yl}carbonyl)amino]benzyl}sulfonyl)propanoate (Example 119, 120 mg, 0.25 mmol) in THF (5 ml) was treated with concentrated HCl (2 ml). After stirring at RT for 48 hours a further portion of concentrated HCl (5 ml) was added. After stirring for a further 72 hours, the solvent was reduced in vacuo to half the volume and the mixture extracted with EtOAc. The combined organic extracts were washed with water, passed through a hydrophobic frit and the solvent removed in vacuo. The residue was purified by column chromatography (silica) eluting with DCM containing increasing amounts of methanol to give the title compound as a white solid (90 mg, 78%).

Workup

  1. additionwas added
  2. extractionthe mixture extracted with EtOAc
  3. washThe combined organic extracts were washed with water
  4. customthe solvent removed in vacuo
  5. customThe residue was purified by column chromatography (silica)
  6. washeluting with DCM containing
  7. temperatureincreasing amounts of methanol

Sources & evidence

ORD record
ord-e8c42e5d687446b4b5af9800c8ef0c1c
Source dataset
uspto-grants-2015_10
Patent number
US09150519B2

Reaction notes

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