ホームMCPワークベンチSkills
ホームワークベンチ通知マイページ
llms.txt · MCPガイドプライバシーポリシー · 利用規約 · サポートv1.8.0
  1. ホーム
  2. /反応

Triethylamine → 3-(2,5-Dimethyl-pyrrol-1-yl)-5,6-bis-trifluoromethyl-pyridine-2-carboxylic acid (3,3,3-trifluoro-2-hydroxy-2-methyl-propyl)-amide

HRID 887843
ノート
印刷プレビュー

反応式

HRID 887843 の反応式
[CH3:1][C:2]1[N:3]([C:8]2[C:9]([C:22]([OH:24])=O)=[N:10][C:11]([C:18]([F:21])([F:20])[F:19])=[C:12]([C:14]([F:17])([F:16])[F:15])[CH:13]=2)[C:4]([CH3:7])=[CH:5][CH:6]=1.Cl.[NH2:26][CH2:27][C:28]([CH3:34])([OH:33])[C:29]([F:32])([F:31])[F:30].CN(C(ON1N=NC2C=CC=NC1=2)=[N+](C)C)C.F[P-](F)(F)(F)(F)F.CCN(CC)CC>CN1C(=O)CCC1>[F:30][C:29]([F:32])([F:31])[C:28]([OH:33])([CH3:34])[CH2:27][NH:26][C:22]([C:9]1[C:8]([N:3]2[C:2]([CH3:1])=[CH:6][CH:5]=[C:4]2[CH3:7])=[CH:13][C:12]([C:14]([F:15])([F:17])[F:16])=[C:11]([C:18]([F:21])([F:19])[F:20])[N:10]=1)=[O:24]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 8471Triethylamine3 回HCID 9886157Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)2 回HCID 584423653-(2,5-Dimethyl-pyrrol-1-yl)-5,6-bis-trifluoromethyl-pyridine-2-carboxylic acid2 回HCID 717573513-Amino-1,1,1-trifluoro-2-methylpropan-2-ol hydrochloride

生成物 1

HCID 86657666
3-(2,5-Dimethyl-pyrrol-1-yl)-5,6-bis-trifluoromethyl-pyridine-2-carboxylic acid (3,3,3-trifluoro-2-hydroxy-2-methyl-propyl)-amide

試薬・触媒・溶媒 1

HCID 13387N-methyl-2-pyrrolidone溶媒

実験手順

To a stirred solution of 3-(2,5-dimethyl-pyrrol-1-yl)-5,6-bis-trifluoromethyl-pyridine-2-carboxylic acid (Intermediate M) (1.16 g, 3.29 mmol) in NMP (32 ml) was added 3-Amino-1,1,1-trifluoro-2-methyl-propan-2-ol hydrochloride (commercially available) (591 mg, 3.29 mmol) followed by HATU (1.25 g, 3.29 mmol) and NEt3 (918 ul, 6.59 mmol) and the reaction mixture was left to stir at RT. After 1 h a further 0.2 equiv. NEt3 was added. After 15 min a further 0.4 equiv. NEt3 and 0.2 equiv. amine were added. After 30 min a further 0.1 equiv HATU was added. After 30 min most of the starting material had been consumed. The reaction mixture was added to EtOAc (50 ml), washed with 0.1M NaOH and the aqueous layer was back extracted with EtOAc (2×50 ml). The combined organic extracts were washed with water (2×150 ml), brine (100 ml), dried (MgSO4) and concentrated in vacuo to give the crude product as an orange oil.

後処理

  1. waitthe reaction mixture was left
  2. waitAfter 15 min a further 0.4 equiv
  3. customAfter 30 min most of the starting material had been consumed
  4. additionThe reaction mixture was added to EtOAc (50 ml)
  5. washwashed with 0.1M NaOH
  6. extractionthe aqueous layer was back extracted with EtOAc (2×50 ml)
  7. washThe combined organic extracts were washed with water (2×150 ml), brine (100 ml)
  8. dry with materialdried (MgSO4)
  9. concentrationconcentrated in vacuo

出典と根拠

ORDレコード
ord-5f0eb78fc2834787a1b1a7bdc3f35b4e
出典データセット
uspto-grants-2012_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08247436B2

反応ノート

読み込み中…

このページの内容参加物実験手順後処理出典と根拠反応ノート