Triethylamine → HCID 11618423、化合物

HRID 2217773ノート

反応式

HRID 2217773 の反応式
[F:1][C:2]1[CH:3]=[C:4]([CH2:9][C:10]([OH:12])=O)[CH:5]=[C:6]([F:8])[CH:7]=1.[C:13]([C:17]1[S:21][C:20]([NH:22][C:23](=[O:29])[CH:24]([NH2:28])[CH2:25][CH2:26][CH3:27])=[N:19][N:18]=1)([CH3:16])([CH3:15])[CH3:14].CCN=C=NCCCN(C)C.Cl.C(N(CC)CC)C>C(Cl)Cl>[C:13]([C:17]1[S:21][C:20]([NH:22][C:23](=[O:29])[CH:24]([NH:28][C:10](=[O:12])[CH2:9][C:4]2[CH:5]=[C:6]([F:8])[CH:7]=[C:2]([F:1])[CH:3]=2)[CH2:25][CH2:26][CH3:27])=[N:19][N:18]=1)([CH3:15])([CH3:14])[CH3:16]

参加物

6

実験手順

A mixture of 3,5-di-fluoro-phenyl acetic acid (51.6 mg, 0.3 mmol), 2-amino-pentanoic acid (5-tert-butyl-[1,3,4]thiadiazol-2-yl)-amide (88 mg, 0.3 mmol), HBOT (43 mg, 0.315 mmol), EDC HCl (69 mg, 0.36 mmol.) and triethylamine (0.17 ml) in methylene chloride was stirred at room temperature until product formation or disappearance of starting material. The mixture was quenched with water and extracted with methylene chloride. The organic layer was separated, washed with dilute HCl, brine, dried over sodium sulfate and the solvent was removed at reduced pressure to provide the title compound as a cude oil. The oil was purified by Shimadzu HPLC to provide the title compound as a white solid (56 mg), LC-MS M+1=411.2, 1H NMR(CDCL3) 8.7 (d,1H,NH), 6.73(m,2H), 6.6(m,1H), 4.7(m,1H), 3.5(Abq, 2H), 1.6-1.9(m,2H), 1.3-1.6(m,2H), 1.5(s,9H), 0.92(t,3H) ppm.

後処理

  1. customThe mixture was quenched with water
  2. extractionextracted with methylene chloride
  3. customThe organic layer was separated
  4. washwashed with dilute HCl, brine
  5. dry with materialdried over sodium sulfate
  6. customthe solvent was removed at reduced pressure

出典と根拠

ORDレコード
ord-181c8279f1564a35bcc0abc35c667ad2
出典データセット
uspto-grants-2008_08
特許番号
US07408068B2

反応ノート

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