تفاعل #1509634

ord-14bda1d1ea59465db8f2510abe686dd1

معادلة التفاعل

O=C(CBr)CCCN1C(=O)c2ccccc2C1=O
1-bromo-5-phthalimido-2-pentanone
NC(N)=S
thiourea
Nc1nc(CCCN2C(=O)c3ccccc3C2=O)cs1
51
المردود 97.0%
Nc1nc(CCCN2C(=O)c3ccccc3C2=O)cs1
2-amino-4-(3-phthalimidopropyl)thiazole
المردود 97.0%

الكواشف

لا شيء

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىthe DMF was removed under reduced pressure
  2. 2
    استخلاصThe aqueous solution was then extracted with EtOAc (3×40 mL)
  3. 3
    غسيلthe organic layer was washed with brine (50 mL)
  4. 4
    تجفيفdried (Na2SO4)
  5. 5
    ترشيحfiltered
  6. 6
    تركيزconcentrated

الإجراء التجريبي

1-bromo-5-phthalimido-2-pentanone (0.500 g, 1.61 mmol) was dissolved in DMF (3.5 mL) at 0° C. and thiourea (0.135 g, 1.77 mmol) was added drop-wise as a solution in DMF (0.50 mL). The solution was allowed to warm to room temperature and stirring was continued for 2 h at which time the DMF was removed under reduced pressure and the resulting slurry was made alkaline with 10% K2CO3 (100 mL). The aqueous solution was then extracted with EtOAc (3×40 mL) and the organic layer was washed with brine (50 mL), dried (Na2SO4), filtered and concentrated to obtain 51 (448 mg, 97%) as a fine white powder in its freebase form: 1H NMR (300 MHz, DMSO-d6) δ 7.85 (m, 4H), 6.78 (s, 2H), 6.13 (s, 1H), 3.56 (t, 2H, J=6.9 Hz), 2.42 (t, 2H, J=7.5 Hz), 1.88 (quint., 2H, J=7.5 Hz); 13C NMR (75 MHz, DMSO-d6) δ 168.01, 167.87, 151.20, 134.25, 131.61, 122.89, 100.17, 37.27, 28.70, 27.09; HRMS (ESI) calcd for C14H14N3O2S (MH+) 288.0801, found 288.0799.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08927029B2uspto-grants-2015_01