Triethylamine → N-[2-amino-4-(6-iodo-1H-indazol-1-yl)pyrimidin-5-yl]-3-methyloxetane-3-carboxamide

HRID 1398495ノート

反応式

HRID 1398495 の反応式
[CH3:1][C:2]1([C:6]([OH:8])=O)[CH2:5][O:4][CH2:3]1.CN(C(ON1N=NC2C=CC=NC1=2)=[N+](C)C)C.F[P-](F)(F)(F)(F)F.[I:33][C:34]1[CH:42]=[C:41]2[C:37]([CH:38]=[N:39][N:40]2[C:43]2[C:48]([NH2:49])=[CH:47][N:46]=[C:45]([NH2:50])[N:44]=2)=[CH:36][CH:35]=1.C(N(CC)CC)C>CN(C=O)C.CCOC(C)=O>[NH2:50][C:45]1[N:44]=[C:43]([N:40]2[C:41]3[C:37](=[CH:36][CH:35]=[C:34]([I:33])[CH:42]=3)[CH:38]=[N:39]2)[C:48]([NH:49][C:6]([C:2]2([CH3:1])[CH2:5][O:4][CH2:3]2)=[O:8])=[CH:47][N:46]=1

参加物

7

実験手順

To a mixture of 3-methyloxetane-3-carboxylic acid (8.7 mg, 0.075 mmol) and HATU (28.5 mg, 0.075 mmol) was added a solution of crude 4-(6-iodo-1H-indazol-1-yl)pyrimidine-2,5-diamine (11% purity, 120 mg, 0.037 mmol) in DMF (0.5 mL) followed by triethylamine (0.016 mL, 0.112 mmol). The mixture was stirred at RT for 10 min, then diluted with EtOAc (10 mL) and washed with water (2×3 mL). The combined organic layer was dried over Na2SO4, filtered and concentrated in vacuo to give the crude compound. Purification by flash chromatography (Isolute column, 100% DCM to 3% MeOH in DCM) gave the title compound; m/z=+451.30 (M+H)+, (purity=76%). This intermediate was used in the next step without further purification.

後処理

  1. washwashed with water (2×3 mL)
  2. dry with materialThe combined organic layer was dried over Na2SO4
  3. filtrationfiltered
  4. concentrationconcentrated in vacuo
  5. customto give the crude compound
  6. customPurification by flash chromatography (Isolute column, 100% DCM to 3% MeOH in DCM)

出典と根拠

ORDレコード
ord-de44690b126c4065b7772c219a60f29d
出典データセット
uspto-grants-2014_12
特許番号
US08901313B2

反応ノート

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