2-Aminoadamantane hydrochloride → 1-tert-butyl-5-trifluoromethyl-1H-pyrazole-4-carboxylic acid adamantan-2-ylamide

HRID 12832

반응식

HRID 12832 반응식
[C:1]([N:5]1[C:9]([C:10]([F:13])([F:12])[F:11])=[C:8]([C:14]([OH:16])=O)[CH:7]=[N:6]1)([CH3:4])([CH3:3])[CH3:2].CCN(C(C)C)C(C)C.[B-](F)(F)(F)F.CN(C(ON1C(=O)CCC1=O)=[N+](C)C)C.Cl.[NH2:47][CH:48]1[CH:55]2[CH2:56][CH:51]3[CH2:52][CH:53]([CH2:57][CH:49]1[CH2:50]3)[CH2:54]2>ClCCl.CN(C=O)C.O>[CH:49]12[CH2:57][CH:53]3[CH2:52][CH:51]([CH2:56][CH:55]([CH2:54]3)[CH:48]1[NH:47][C:14]([C:8]1[CH:7]=[N:6][N:5]([C:1]([CH3:2])([CH3:3])[CH3:4])[C:9]=1[C:10]([F:11])([F:12])[F:13])=[O:16])[CH2:50]2

참가 물질

8

실험 절차

tert-Butyl-5-trifluoromethyl-1H-pyrazole-4-carboxylic acid (Intermediate 7, 61 mg, 0.26 mmol) was dissolved in a mixture of dry dichloromethane (3.2 mL) and dry DMF (0.8 mL). DIPEA (0.23 mL, 1.3 mmol) and TSTU (93 mg, 0.28 mmol) were added to the above mixture. After the mixture was stirred for 1 h, the appearance of active ester was detected by LC-MS. Then 2-aminoadamantane hydrochloride (58 mg, 0.31 mmol) was added. After another 2 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 and purified by C-18 reversed phase HPLC with a gradient of 10-100% acetonitrile/water to give 1-tert-butyl-5-trifluoromethyl-1H-pyrazole-4-carboxylic acid adamantan-2-ylamide (62 mg, 65%). Mass spectrum: m/z: 370.2 (M+1).

후처리

  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. custompurified by C-18

출처 및 근거

ORD 기록
ord-d53e24288b474cab86af0923b73f4cca
출처 데이터셋
uspto-grants-2010_06
특허 번호
US07728029B2

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