반응 #10897

ord-b17a0c7b6d284d0a959d2f696bb214cf

반응 방정식

O=C(CBr)c1ccc(N2CCCC2)cc1
2-Bromo-1-[4-(1-pyrrolidinyl)phenyl]ethanone
CN1CCN(c2ccc(N=C=S)cc2)CC1
1-(4-isothiocyanatophenyl)-4-methyl piperazine
CN1CCN(c2ccc(N=C=S)cc2)CC1
1-(4-isothiocyanatophenyl)-4-methylpiperazine
N#CN
cyanamide
CC(C)(C)[O-].[K+]
Potassium t-butoxide
CN1CCN(c2ccc(Nc3nc(N)c(C(=O)c4ccc(N5CCCC5)cc4)s3)cc2)CC1
[4-amino-2-[[4-(4-methyl-1-piperazinyl)phenyl]amino]-5-thiazolyl][4-(1-pyrrolidinyl) phenyl]methanone
수율 4.0%

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    workup.STIRRINGthe solution was stirred at room temperature for 2 days
  2. 2
    여과The yellow-brown solid was filtered off
  3. 3
    세척washed with cold acetonitrile, water
  4. 4
    기타A portion of this crude product (50 mg) was purified by chromatography (10% methanol/dichloromethane)

실험 절차

tert-Butanol (4 mL) and then 1-(4-isothiocyanatophenyl)-4-methyl piperazine (of Example 1; 219 mg, 1 mmol) were added to a solution of cyanamide (44 mg, 1.05 mmol) in acetonitrile (5 mL). Potassium t-butoxide (1 M in tert-butanol; 1 mL, 1 mmol) was added and the solution was stirred for 30 min. 2-Bromo-1-[4-(1-pyrrolidinyl)phenyl]ethanone (257 mg, 1 mmol) (Lancaster) was added, and the solution was stirred at room temperature for 2 days. The yellow-brown solid was filtered off and washed with cold acetonitrile, water and then cold acetonitrile (weight of solid: 271 mg). A portion of this crude product (50 mg) was purified by chromatography (10% methanol/dichloromethane) to give [4-amino-2-[[4-(4-methyl-1-piperazinyl)phenyl]amino]-5-thiazolyl][4-(1-pyrrolidinyl) phenyl]methanone (18.5 mg).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07094896B2uspto-grants-2006_08