Diisopropylethylamine → HCID 67500744、化合物

HRID 1631369ノート

反応式

HRID 1631369 の反応式
[F:1][C:2]1[CH:3]=[C:4]([C@H:8]2[CH2:12][CH2:11][CH2:10][N:9]2[C:13]2[CH:18]=[CH:17][N:16]3[N:19]=[CH:20][C:21]([C:22]([OH:24])=O)=[C:15]3[N:14]=2)[CH:5]=[N:6][CH:7]=1.CN(C(ON1N=[N:40][C:35]2[CH:36]=[CH:37]C=N[C:34]1=2)=[N+](C)C)C.F[P-](F)(F)(F)(F)F.Cl.CC1(N)CC1.CCN(C(C)C)C(C)C>CN(C=O)C>[F:1][C:2]1[CH:3]=[C:4]([C@H:8]2[CH2:12][CH2:11][CH2:10][N:9]2[C:13]2[CH:18]=[CH:17][N:16]3[N:19]=[CH:20][C:21]([C:22]([NH:40][C:35]4([CH3:34])[CH2:37][CH2:36]4)=[O:24])=[C:15]3[N:14]=2)[CH:5]=[N:6][CH:7]=1

参加物

6

実験手順

To a DMF (0.6 mL) solution of (R)-5-(2-(5-fluoropyridin-3-yl)pyrrolidin-1-yl)pyrazolo[1,5-a]pyrimidine-3-carboxylic acid (Preparation I, 10.5 mg, 0.0321 mmol) and HATU (14.6 mg, 0.0385 mmol) was added 1-methylcyclopropanamine hydrochloride (4.14 mg, 0.0385 mmol) and DIEA (0.0168 mL, 0.0962 mmol). After stirring for 10 minutes, the reaction mixture was directly purified by reverse-phase chromatography (5 to 50% acetonitrile/water) to yield the final product as white solid (10 mg, 82%). LCMS (apci) m/z=381.1 (M+H).

後処理

  1. customthe reaction mixture was directly purified by reverse-phase chromatography (5 to 50% acetonitrile/water)

出典と根拠

ORDレコード
ord-b4bc8da7895f497bb9c9a1d4ebca1eaa
出典データセット
uspto-grants-2014_07
特許番号
US08791123B2

反応ノート

読み込み中…