Formamide → HCID 178461168, compound

HRID 527217Notes

Reaction equation

HRID 527217 reaction equation
[NH2:1][C:2]1[CH2:6][CH2:5][C@@H:4]([CH3:7])[C:3]=1[C:8]([O:10]CC)=O.C([O-])=O.[NH4+].[CH:17]([NH2:19])=O>>[CH3:7][C@H:4]1[C:3]2[C:8]([OH:10])=[N:19][CH:17]=[N:1][C:2]=2[CH2:6][CH2:5]1

Participants

4

Conditions

Temperature
150 °C

Procedure

A solution containing (R)-ethyl 2-amino-5-methylcyclopent-1-enecarboxylate (161.61 g, 955.024 mmol) and ammonium formate (90.3298 g, 1432.54 mmol) in formamide (303.456 ml, 7640.19 mmol) was heated to an internal temperature of 150° C. and stirred for 17 hours. The reaction mixture was cooled, and transferred to a 2 L single neck flask. Then excess formamidine was removed by high vacuum distillation. Once formamidine stopped coming over, the remaining oil in the still pot was dissolved in DCM and washed with brine (3×200 mL) The combined aqueous washes were extracted with DCM. The combined organic extracts were dried (Na2SO4), filtered, and concentrated. The resulting brown oil was dissolved in minimal DCM, and this solution was added using a separatory funnel to a stirred solution of ether (ca. 5 vol of ether vs. DCM solution), causing some brown precipitate to form. This brown precipitate was removed by filtration through a medium frit funnel which was rinsed with ether and disposed. The filtrate was concentrated, the trituration from ether repeated two more times and then dried on high vacuum line to give (R)-5-methyl-6,7-dihydro-5H-cyclopenta[d]pyrimidin-4-ol (93.225 g, 65.00% yield) as a brown-yellow pasty solid. LC/MS (APCI−) m/z 149.2.

Workup

  1. temperatureThe reaction mixture was cooled
  2. customtransferred to a 2 L single neck flask
  3. customThen excess formamidine was removed by high vacuum distillation
  4. dissolutionpot was dissolved in DCM
  5. washwashed with brine (3×200 mL) The combined aqueous washes
  6. extractionwere extracted with DCM
  7. dry with materialThe combined organic extracts were dried (Na2SO4)
  8. filtrationfiltered
  9. concentrationconcentrated
  10. dissolutionThe resulting brown oil was dissolved in minimal DCM
  11. additionthis solution was added
  12. customto form
  13. customThis brown precipitate was removed by filtration through a medium frit funnel which
  14. washwas rinsed with ether
  15. concentrationThe filtrate was concentrated
  16. customdried on high vacuum line

Sources & evidence

ORD record
ord-f16f28c685a14340bfe34e37ad7927dc
Source dataset
uspto-grants-2016_05
Patent number
US09346789B2

Reaction notes

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