Dicyclohexylcarbodiimide → HCID 54547844, 화합물

HRID 582286노트

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HRID 582286 반응식
[CH3:1][O:2][C:3]1[CH:4]=[C:5]([NH:9][C:10]2[CH:18]=[CH:17][CH:16]=[CH:15][C:11]=2C(O)=O)[CH:6]=[CH:7][CH:8]=1.[OH:19]N1C2C=CC=CC=2N=N1.N1CCCC1.C1(N=[C:41]=[N:42][CH:43]2CC[CH2:46][CH2:45][CH2:44]2)CCCCC1>C1COCC1.CC#N.C(Cl)Cl>[CH3:1][O:2][C:3]1[CH:4]=[C:5]([NH:9][C:10]2[CH:11]=[CH:15][C:16]([C:41]([N:42]3[CH2:43][CH2:44][CH2:45][CH2:46]3)=[O:19])=[CH:17][CH:18]=2)[CH:6]=[CH:7][CH:8]=1

참가 물질

7

반응물 4

HCID 10868DicyclohexylcarbodiimideHCID 31268PyrrolidineHCID 757711-HydroxybenzotriazoleHCID 119702Anthranilic acid, N-(3-methoxyphenyl)-

생성물 1

HCID 54547844HCID 54547844, 화합물

시약·촉매·용매 2

HCID 6344Dichloromethane용매HCID 22177404Acetonitrile tetrahydrofuran용매

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온도
0 °C

실험 절차

2 g (8.2 mmol) of 4-[N-(3-methoxyphenyl)aminobenzoic acid, 2.2 g (16.4 mmol) of N-hydroxybenzotriazole and 1 ml (12.3 mmol) of pyrrolidine were dissolved in 40 ml of a 7:3 mixture of THF/CH3CN, under a nitrogen atmosphere. The solution was cooled to 0° C. and 3.4 g (16.4 mmol) of dicyclohexylcarbodiimide dissolved in 20 ml of CH2Cl2 were added. The reaction mixture was allowed to warm to room temperature during 1 h., stirred an additional hour, then the precipitate was filtered off and the solvent was removed in vacuo. The residue was taken up with water and extracted with AcOEt, the organic layer was dried over Na2SO4 and the solvent removed in vacuo. The resulting crude mixture was purified by flash chromatography (AcOEt), yielding 2.4 g of the title compound.

후처리

  1. additionwere added
  2. temperatureto warm to room temperature during 1 h.
  3. filtrationthe precipitate was filtered off
  4. customthe solvent was removed in vacuo
  5. extractionextracted with AcOEt
  6. dry with materialthe organic layer was dried over Na2SO4
  7. customthe solvent removed in vacuo
  8. customThe resulting crude mixture was purified by flash chromatography (AcOEt)

출처 및 근거

ORD 기록
ord-754f0d4c459c4e6083767e74408182d4
출처 데이터셋
uspto-grants-1999_07
특허 번호
US05922887

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