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Diethylamine → HCID 28814207, 화합물

HRID 423077
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HRID 423077 반응식
[CH2:1]([NH:3][CH2:4][CH3:5])[CH3:2].CS(O[CH2:11][CH2:12][C@H:13]([NH:21]C(OC(C)(C)C)=O)[C:14]1[CH:19]=[CH:18][C:17]([Cl:20])=[CH:16][CH:15]=1)(=O)=O>C1COCC1>[Cl:20][C:17]1[CH:16]=[CH:15][C:14]([C@@H:13]([NH2:21])[CH2:12][CH2:11][N:3]([CH2:4][CH3:5])[CH2:1][CH3:2])=[CH:19][CH:18]=1
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참가 물질

4

반응물 2

HCID 8021DiethylamineHCID 57750320(S)-3-(tert-butoxycarbonylamino)-3-(4-chlorophenyl)propyl methanesulfonate2회

생성물 1

HCID 28814207HCID 28814207, 화합물수율 36.1%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

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온도
120 °C

실험 절차

Diethylamine (0.426 mL, 4.12 mmol) and (S)-3-(tert-butoxycarbonylamino)-3-(4-chlorophenyl)propyl methanesulfonate (Intermediate 59) (500 mg, 1.37 mmol) were dissolved in THF (10 mL) and sealed into a microwave tube. The reaction was heated to 120° C. for 50 minutes in the microwave reactor and cooled to room temperature. The reaction mixture was concentrated and diluted with DCM (5 mL). TFA (1 mL) was added and the reaction was stirred at 20° C. for 1 hour. The crude product was purified by ion exchange chromatography, using an SCX column. The desired product was eluted from the column using 3.5N ammonia/MeOH and pure fractions were evaporated to dryness to afford (S)-1-(4-chlorophenyl)-N3,N3-diethylpropane-1,3-diamine (119 mg, 36.0%) as a yellow oil.

후처리

  1. customsealed into a microwave tube
  2. temperaturecooled to room temperature
  3. concentrationThe reaction mixture was concentrated
  4. additiondiluted with DCM (5 mL)
  5. additionTFA (1 mL) was added
  6. customThe crude product was purified by ion exchange chromatography
  7. washThe desired product was eluted from the column
  8. customwere evaporated to dryness

출처 및 근거

ORD 기록
ord-77e2bee07dfe4735a093d72eb1214788
출처 데이터셋
uspto-grants-2012_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08101623B2

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