تفاعل #327484

ord-8d9733a562a74514989aa817119a1711

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    ترشيحfiltered
  2. 2
    workup.ADDITIONadded to the resin
  3. 3
    ترشيحThe resin was filtered
  4. 4
    غسيلwashed with DCM:MeOH:DIPEA (17:2:1), DCM, NMP og DCM (2×25 mL of each)
  5. 5
    workup.WAITThe resin was swelled in NMP for 20 mins
  6. 6
    ترشيحfiltered
  7. 7
    workup.STIRRINGthe resin was shaken for 90 min at RT
  8. 8
    workup.STIRRINGThe resin was shaken for overnigth
  9. 9
    ترشيحThe resin was filtered
  10. 10
    غسيلwashed with NMP (5×20 mL) and DCM (10×20 mL)
  11. 11
    workup.ADDITIONTFA/TIS/water (95:2.5:2.5; 30 mL) was added to the resin and it
  12. 12
    workup.WAITwas shaked for 1 hr
  13. 13
    ترشيحfiltered
  14. 14
    تركيزconcentrated in vacuo

الإجراء التجريبي

Chlorotrityl chloride resin (2.3 g, 3.0 mmol) was swelled in DCM for 20 mins and filtered. Dimethylmalonic acid (2 eq; 6.0 mmol; 793 mg) was dissolved i DCM:NMP 1:1 (10 mL) and added to the resin followed by DIPEA (6 eq; 18.0 mmol; 3.14 mL) and DCM (10 mL). The resin was shaken overnight at RT. The resin was filtered and washed with DCM:MeOH:DIPEA (17:2:1), DCM, NMP og DCM (2×25 mL of each). The resin was swelled in NMP for 20 mins and filtered. HOAt (3 eq; 9.0 mmol; 1.23 g), DIC (3 eq; 9.0 mmol; 1.40 mL) and NMP (25 mL) was added and the resin was shaken for 90 min at RT. The resin was filtrered and 2-(Aminomethyl)pyridine (2 eq; 6 mmol; 659 mg), DIPEA (4 eq; 6.0 mmol; 2.09 mL), and NMP (10 mL) was added. The resin was shaken for overnigth. The resin was filtered and washed with NMP (5×20 mL) and DCM (10×20 mL). TFA/TIS/water (95:2.5:2.5; 30 mL) was added to the resin and it was shaked for 1 hr, filtered and concentrated in vacuo to yield the title compound.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08648041B2uspto-grants-2014_02