Diisopropylethylamine → HCID 67314100, 화합물

HRID 2179583노트

반응식

HRID 2179583 반응식
[C:1]([C:3]1[CH:14]=[CH:13][C:6]2[CH:7]=[C:8]([C:10]([OH:12])=O)[S:9][C:5]=2[CH:4]=1)#[N:2].[ClH:15].Cl.[NH2:17][C@@H:18]1[CH:23]2[CH2:24][CH2:25][N:20]([CH2:21][CH2:22]2)[CH2:19]1.CN(C(ON1N=NC2C=CC=NC1=2)=[N+](C)C)C.F[P-](F)(F)(F)(F)F.C(N(CC)C(C)C)(C)C>CN(C=O)C>[ClH:15].[N:20]12[CH2:25][CH2:24][CH:23]([CH2:22][CH2:21]1)[C@@H:18]([NH:17][C:10]([C:8]1[S:9][C:5]3[CH:4]=[C:3]([C:1]#[N:2])[CH:14]=[CH:13][C:6]=3[CH:7]=1)=[O:12])[CH2:19]2

참가 물질

6

실험 절차

320.8 mg (1.1 mmol) of 6-cyano-1-benzothiophene-2-carboxylic acid (Example 25A), 200 mg (1.0 mmol) of (R)-3-aminoquinuclidine dihydrochloride, 458.3 mg (1.21 mmol) of HATU, 467.3 mg (3.62 mmol) of N,N-diisopropylethylamine and 4.0 ml of DMF are reacted by general method C. The reaction mixture is purified by preparative HPLC. The product is dissolved in a mixture of methanol and 4 M hydrogen chloride in dioxane and then concentrated and dried under high vacuum. 222.1 mg (64% of theory) of the title compound are obtained.

후처리

  1. customThe reaction mixture is purified by preparative HPLC
  2. dissolutionThe product is dissolved in a mixture of methanol and 4 M hydrogen chloride in dioxane
  3. concentrationconcentrated
  4. customdried under high vacuum

출처 및 근거

ORD 기록
ord-63d9f822cff14d72a5b391374cf07612
출처 데이터셋
uspto-grants-2015_06
특허 번호
US09067931B2

반응 노트

불러오는 중…