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Trimethylaluminum → HCID 178489784, 화합물

HRID 1911480
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HRID 1911480 반응식
C[Al](C)C.[CH:5]1([N:8]2[CH2:14][CH2:13][CH2:12][N:11]([C:15]3[N:20]=[CH:19][C:18]([C:21]([O:23]C)=O)=[CH:17][N:16]=3)[CH2:10][CH2:9]2)[CH2:7][CH2:6]1.[CH3:25][O:26][C:27]1[CH:28]=[C:29]([CH2:35][CH2:36][C:37]2[CH:38]=[C:39]([NH2:42])[NH:40][N:41]=2)[CH:30]=[C:31]([O:33][CH3:34])[CH:32]=1>C1(C)C=CC=CC=1>[CH:5]1([N:8]2[CH2:14][CH2:13][CH2:12][N:11]([C:15]3[N:16]=[CH:17][C:18]([C:21]([NH:42][C:39]4[NH:40][N:41]=[C:37]([CH2:36][CH2:35][C:29]5[CH:30]=[C:31]([O:33][CH3:34])[CH:32]=[C:27]([O:26][CH3:25])[CH:28]=5)[CH:38]=4)=[O:23])=[CH:19][N:20]=3)[CH2:10][CH2:9]2)[CH2:6][CH2:7]1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 16682925TrimethylaluminumHCID 66589974Methyl 2-(4-cyclopropyl-1,4-diazepan-1-yl)pyrimidine-5-carboxylateHCID 178489815HCID 178489815, 화합물

생성물 1

HCID 178489784HCID 178489784, 화합물수율 1.5%

시약·촉매·용매 1

HCID 1140Toluene용매

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온도
60 °C

실험 절차

Trimethylaluminium (1.402 ml, 2.80 mmol) was added dropwise to a stirred suspension of methyl 2-(4-cyclopropyl-1,4-diazepan-1-yl)pyrimidine-5-carboxylate (310 mg, 1.12 mmol) and 5-[2-(3,5-dimethoxyphenyl)ethyl]-2H-pyrazol-3-amine (277 mg, 1.12 mmol) in toluene (5.61 ml) at 25° C. The resulting solution was stirred at 60° C. for 18 h. The cooled reaction mixture was quenched into methanol (50 mL) and treated with HCl (2M aqueous solution, to pH7 or lower) and purified by ion exchange chromatography, using a SCX column. The desired product was eluted from the column using 7M NH3/MeOH and evaporated to dryness to afford impure product. The crude product was purified by preparative HPLC, using decreasingly polar mixtures of water (containing 1% NH3) and MeCN as eluents. Fractions containing the desired compound were evaporated to dryness to afford the title compound (8.00 mg, 1%) as a cream solid. Some impure fractions were combined and concentrated to dryness and purified by crystallisation from MeCN to afford the title compound (51 mg, 9%) as a cream solid.

후처리

  1. customThe cooled reaction mixture
  2. customwas quenched into methanol (50 mL)
  3. additiontreated with HCl (2M aqueous solution, to pH7 or lower)
  4. custompurified by ion exchange chromatography
  5. washThe desired product was eluted from the column
  6. customevaporated to dryness
  7. customto afford impure product
  8. customThe crude product was purified by preparative HPLC
  9. additionFractions containing the desired compound
  10. customwere evaporated to dryness

출처 및 근거

ORD 기록
ord-55d897091436495d8fb8bf83144ce9f3
출처 데이터셋
uspto-grants-2013_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08604022B2

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