8-Azaspiro[4.5]decane-8-sulfonyl chloride → Methyl (S)-2-(8-azaspiro[4.5]decane-8-sulfonylamino)-4,4-difluoropentanoate

HRID 1664736노트

반응식

HRID 1664736 반응식
Cl.[NH2:2][C@@H:3]([CH2:8][C:9]([F:12])([F:11])[CH3:10])[C:4]([O:6][CH3:7])=[O:5].[CH2:13]1[C:17]2([CH2:22][CH2:21][N:20]([S:23](Cl)(=[O:25])=[O:24])[CH2:19][CH2:18]2)[CH2:16][CH2:15][CH2:14]1>C(#N)C>[CH2:13]1[C:17]2([CH2:18][CH2:19][N:20]([S:23]([NH:2][C@@H:3]([CH2:8][C:9]([F:11])([F:12])[CH3:10])[C:4]([O:6][CH3:7])=[O:5])(=[O:25])=[O:24])[CH2:21][CH2:22]2)[CH2:16][CH2:15][CH2:14]1

참가 물질

4

실험 절차

In a reaction vessel, 100 mg of methyl (S)-2-amino-4,4-difluoropentanoate hydrochloride (0.49 mmol) were admixed with 320 mg of N,O-bis(trimethylsilyl)-acetamide (3.2 eq.) in 3 ml of acetonitrile. The reaction mixture was treated at 100° C. in a microwave for 30 min. 128 mg of 8-azaspiro[4.5]decane-8-sulfonyl chloride (1.1 eq.), dissolved in 2.5 ml of acetonitrile, were then added and the resulting reaction mixture was treated at 100° C. in a microwave for a further 2.5 h. The reaction mixture was concentrated under reduced pressure and the resulting residue was purified by preparative HPLC (gradient: acetonitrile/water and addition of 0.05% TFA). Methyl (S)-2-(8-azaspiro[4.5]decane-8-sulfonylamino)-4,4-difluoropentanoate was obtained as a colorless amorphous material.

후처리

  1. additionThe reaction mixture was treated at 100° C. in a microwave for 30 min
  2. additionwere then added
  3. customthe resulting reaction mixture
  4. additionwas treated at 100° C. in a microwave for a further 2.5 h
  5. concentrationThe reaction mixture was concentrated under reduced pressure
  6. customthe resulting residue was purified by preparative HPLC (gradient: acetonitrile/water and addition of 0.05% TFA)

출처 및 근거

ORD 기록
ord-ef66b737ae184ca7ad9b7ab207754d98
출처 데이터셋
uspto-grants-2011_10
특허 번호
US08039480B2

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