Diisopropylethylamine → 1-cyclopropyl-5-trifluoromethyl-1H-pyrazole-4-carboxylic acid (5-hydroxy-adamantan-2-yl)-amide

HRID 12836

反応式

HRID 12836 の反応式
[CH:1]1([N:4]2[C:8]([C:9]([F:12])([F:11])[F:10])=[C:7]([C:13]([OH:15])=O)[CH:6]=[N:5]2)[CH2:3][CH2:2]1.CCN(C(C)C)C(C)C.[B-](F)(F)(F)F.CN(C(ON1C(=O)CCC1=O)=[N+](C)C)C.[NH2:45][CH:46]1[CH:53]2[CH2:54][C:49]3([OH:56])[CH2:50][CH:51]([CH2:55][CH:47]1[CH2:48]3)[CH2:52]2>ClCCl.CN(C=O)C.O>[OH:56][C:49]12[CH2:54][CH:53]3[CH2:52][CH:51]([CH2:55][CH:47]([CH:46]3[NH:45][C:13]([C:7]3[CH:6]=[N:5][N:4]([CH:1]4[CH2:2][CH2:3]4)[C:8]=3[C:9]([F:10])([F:11])[F:12])=[O:15])[CH2:48]1)[CH2:50]2

参加物

8

実験手順

1-Cyclopropyl-5-trifluoromethyl-1H-pyrazole-4-carboxylic acid (Intermediate 6, 100 mg, 0.45 mmol) was dissolved in a mixture of dry dichloromethane (4 mL) and dry DMF (1 mL). DIPEA (0.5 mL, 2.9 mmol) and TSTU (165 mg, 0.5 mmol) were added to the above mixture. After the mixture was stirred for 2 h, the appearance of active ester was detected by LC-MS. Then 4-amino-adamantan-1-ol (77 mg, 0.46 mmol) was added. After another 4 hours water was added and the organic layer was separated. The aqueous layer was extracted twice with dichloromethane. The combined organic layers were dried under vacuum. The crude mixture was purified by C-18 reversed phase preparative-HPLC with a gradient of 10-100% acetonitrile/water to give 1-cyclopropyl-5-trifluoromethyl-1H-pyrazole-4-carboxylic acid (5-hydroxy-adamantan-2-yl)-amide (79 mg, 48%. Mass spectrum: m/z: 370.2 (M+1).

後処理

  1. customthe organic layer was separated
  2. extractionThe aqueous layer was extracted twice with dichloromethane
  3. customThe combined organic layers were dried under vacuum
  4. customThe crude mixture was purified by C-18

出典と根拠

ORDレコード
ord-1d5669c1dacf4500b4f798b19027bbba
出典データセット
uspto-grants-2010_06
特許番号
US07728029B2

関連ノート

読み込み中…