Triethylamine → HCID 11258649, 화합물

HRID 1833264노트

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HRID 1833264 반응식
[CH3:1][O:2][C:3]1[CH:4]=[C:5]2[C:10](=[CH:11][C:12]=1[O:13][CH3:14])[C:9]([C:15](=[O:24])[C:16]1[CH:21]=[CH:20][CH:19]=[C:18]([O:22][CH3:23])[CH:17]=1)=[N:8][CH:7]=[C:6]2[C:25](O)=[O:26].C(N(CC)CC)C.C(OC(Cl)=O)C(C)C.C(O)(=O)/C=C/C(O)=O.[NH2:51][CH2:52][CH2:53][C:54]#[N:55].C(=O)(O)[O-].[Na+]>CN(C)C=O>[C:52]([CH2:53][CH2:54][NH:55][C:25]([C:6]1[C:5]2[C:10](=[CH:11][C:12]([O:13][CH3:14])=[C:3]([O:2][CH3:1])[CH:4]=2)[C:9]([C:15](=[O:24])[C:16]2[CH:21]=[CH:20][CH:19]=[C:18]([O:22][CH3:23])[CH:17]=2)=[N:8][CH:7]=1)=[O:26])#[N:51]

참가 물질

7

실험 절차

A solution of 6,7-dimethoxy-1-(3-methoxy-benzoyl)-isoquinoline-4-carboxylic acid (170 mg, 0.46 mmol) in dry, N,N-dimethylformamide (5 mL) was chilled in an ice bath under argon. With stirring, triethylamine (97 uL, 0.69 mmol) and isobutylchloroformate (72 uL, 0.56 uL) were added. The solution was stirred for 30 min and then 3-aminopropionitrile fumarate (118 mg, 0.92 mmol) and triethylamine (250 uL, 1.79 mmol) were added. The solution was allowed to warmed to room temperature with stirring overnight. The reaction mixture was poured into a 2% aqueous sodium bicarbonate solution (50 mL) and extracted with ethyl acetate (3×25 mL). The combined ethyl acetate layers were dried over magnesium sulfate, filtered and concentrated in vacuo to afford 107 mg (55%) of an off white solid and used without further purification: APCI-MS m/e calcd for C23H21N3O5(M−H+) 420.4, found 420.0; 1H NMR (300 MHz) compatible.

후처리

  1. stirringThe solution was stirred for 30 min
  2. stirringwith stirring overnight
  3. extractionextracted with ethyl acetate (3×25 mL)
  4. dry with materialThe combined ethyl acetate layers were dried over magnesium sulfate
  5. filtrationfiltered
  6. concentrationconcentrated in vacuo
  7. customto afford 107 mg (55%) of an off white solid
  8. customused without further purification

출처 및 근거

ORD 기록
ord-8dd6b8bc79f8489ea7b95f33350e8edf
출처 데이터셋
uspto-grants-2006_06
특허 번호
US07067529B2

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