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Diisopropylethylamine → (2S,4R)-methyl 4-(6-amino-5-(4-(((S)-1-(3-chlorophenyl)-2-hydroxyethyl)carbamoyl)-3-fluorophenyl)pyridin-3-yl)pyrrolidine-2-carboxylate

HRID 596108
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HRID 596108 반응식
[OH:1][C:2]([C:4](F)(F)F)=[O:3].O[C:9](C(F)(F)F)=O.[NH2:15][C:16]1[C:21]([C:22]2[CH:30]=[CH:29][C:25]([C:26](O)=[O:27])=[C:24]([F:31])[CH:23]=2)=[CH:20][C:19]([C@H:32]2[CH2:36][C@@H](C(OC)=O)[NH:34][CH2:33]2)=[CH:18][N:17]=1.CN(C(ON1N=NC2C=CC=NC1=2)=[N+](C)C)C.F[P-](F)(F)(F)(F)F.CCN(C(C)C)C(C)C.[NH2:74][C@@H:75]([C:78]1[CH:83]=[CH:82][CH:81]=[C:80]([Cl:84])[CH:79]=1)[CH2:76][OH:77]>CN(C=O)C>[NH2:15][C:16]1[N:17]=[CH:18][C:19]([C@@H:32]2[CH2:33][NH:34][C@H:4]([C:2]([O:1][CH3:9])=[O:3])[CH2:36]2)=[CH:20][C:21]=1[C:22]1[CH:30]=[CH:29][C:25]([C:26](=[O:27])[NH:74][C@@H:75]([C:78]2[CH:83]=[CH:82][CH:81]=[C:80]([Cl:84])[CH:79]=2)[CH2:76][OH:77])=[C:24]([F:31])[CH:23]=1
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참가 물질

6

반응물 4

HCID 81531DiisopropylethylamineHCID 9886157Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 59694427(S)-2-amino-2-(3-chlorophenyl)ethanolHCID 1317346254-(2-amino-5-((3R,5S)-5-(methoxycarbonyl)pyrrolidin-3-yl)pyridin-3-yl)-2-fluorobenzoic acid-2TFA

생성물 1

HCID 118045925
(2S,4R)-methyl 4-(6-amino-5-(4-(((S)-1-(3-chlorophenyl)-2-hydroxyethyl)carbamoyl)-3-fluorophenyl)pyridin-3-yl)pyrrolidine-2-carboxylate
수율 13.6%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

A mixture of 4-(2-amino-5-((3R,5S)-5-(methoxycarbonyl)pyrrolidin-3-yl)pyridin-3-yl)-2-fluorobenzoic acid-2TFA (35 mg, 0.060 mmol), HATU (34 mg, 0.089 mmol), and DIEA (0.104 mL, 0.596 mmol) in DMF (2 mL) was treated with (S)-2-amino-2-(3-chlorophenyl)ethanol (51 mg, 0.348 mmol). At completion, the reaction was washed with water and brine, then dried over MgSO4 and concentrated. The crude material was purified by reverse phase prep HPLC to provide (2S,4R)-methyl 4-(6-amino-5-(4-(((S)-1-(3-chlorophenyl)-2-hydroxyethyl)carbamoyl)-3-fluorophenyl)pyridin-3-yl)pyrrolidine-2-carboxylate (4.2 mg, 9%). LCMS (m/z): 513.2, 515.2 (MH+), 0.58 min; 1H NMR (400 MHz, CD3OD) δ ppm 7.97-7.86 (m, 3H), 7.49-7.40 (m, 3H), 7.39-7.34 (m, 2H), 7.33-7.26 (m, 1H), 5.19 (t, J=5.87 Hz, 1H), 4.62 (dd, J=7.63, 10.76 Hz, 1H), 3.93-3.77 (m, 6H), 3.74-3.61 (m, 1H), 2.87 (td, J=6.90, 13.21 Hz, 1H), 2.33-2.21 (m, 1H).

후처리

  1. washAt completion, the reaction was washed with water and brine
  2. dry with materialdried over MgSO4
  3. concentrationconcentrated
  4. customThe crude material was purified by reverse phase prep HPLC

출처 및 근거

ORD 기록
ord-f7024074b5e6447bb5d733f6751b308e
출처 데이터셋
uspto-grants-2016_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09242996B2

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