Dichloromethane methanol → 1-(4-Trityloxy-but-2-enyl)-1H-pyrimidine-2,4-dione

HRID 908507Notes

Reaction equation

HRID 908507 reaction equation
C([N:9]1[C:14](=[O:15])[CH:13]=[CH:12][N:11]([CH2:16]/[CH:17]=[CH:18]\[CH2:19][O:20][C:21]([C:34]2[CH:39]=[CH:38][CH:37]=[CH:36][CH:35]=2)([C:28]2[CH:33]=[CH:32][CH:31]=[CH:30][CH:29]=2)[C:22]2[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=2)[C:10]1=[O:40])(=O)C1C=CC=CC=1.C(Cl)Cl.CO>CO[Na].CO>[C:21]([O:20][CH2:19][CH:18]=[CH:17][CH2:16][N:11]1[CH:12]=[CH:13][C:14](=[O:15])[NH:9][C:10]1=[O:40])([C:22]1[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=1)([C:28]1[CH:29]=[CH:30][CH:31]=[CH:32][CH:33]=1)[C:34]1[CH:35]=[CH:36][CH:37]=[CH:38][CH:39]=1

Participants

4

Procedure

A suspension of compound (2) (50 mg; 0.095 mmol) in MeONa/MeOH 0.2 M (5 ml) was stirred at room temperature for 24 hours. During such period of time the suspension became a colourless solution and the TLC (DCM/MeOH 90:10) showed the complete disappearance of the starting amide, and the presence of a new spot at lower Rf. The solution was neutralised with Dowex ion exchange resin. The resin was filtered off and washed twice with MeOH (5 ml). The filtrate was concentrated under reduced pressure and purified by flash chromatography using MeOH/DCM 10:90 as eluent which gave the title compound as a white solid (38 mg, 90%). Rf: 0.66 in DCM/MeOH 90:10.

Workup

  1. waitDuring such period of time the suspension became
  2. filtrationThe resin was filtered off
  3. washwashed twice with MeOH (5 ml)
  4. concentrationThe filtrate was concentrated under reduced pressure
  5. custompurified by flash chromatography

Sources & evidence

ORD record
ord-c3c808e1407346f199f8892be43f3afa
Source dataset
uspto-grants-2011_09
Patent number
US08017620B2

Reaction notes

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