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

Trifluoroacetic acid → N-(azetidin-3-yl)-2-[[7-(pentafluoroethyl)isoquinolin-1-yl]amino]acetamide

HRID 1896964
ノート
印刷プレビュー

反応式

HRID 1896964 の反応式
[F:1][C:2]([F:33])([C:7]1[CH:16]=[C:15]2[C:10]([CH:11]=[CH:12][N:13]=[C:14]2[NH:17][CH2:18][C:19]([NH:21][CH:22]2[CH2:25][N:24](C(OC(C)(C)C)=O)[CH2:23]2)=[O:20])=[CH:9][CH:8]=1)[C:3]([F:6])([F:5])[F:4].C(O)(C(F)(F)F)=O>ClCCl>[NH:24]1[CH2:25][CH:22]([NH:21][C:19](=[O:20])[CH2:18][NH:17][C:14]2[C:15]3[C:10](=[CH:9][CH:8]=[C:7]([C:2]([F:1])([F:33])[C:3]([F:6])([F:4])[F:5])[CH:16]=3)[CH:11]=[CH:12][N:13]=2)[CH2:23]1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 6422Trifluoroacetic acidHCID 86660469Tert-butyl 3-(2-[[7-(pentafluoroethyl)isoquinolin-1-yl]amino]acetamido)azetidine-1-carboxylate

生成物 1

HCID 86660470N-(azetidin-3-yl)-2-[[7-(pentafluoroethyl)isoquinolin-1-yl]amino]acetamide

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

反応条件

温度
0 °C

実験手順

Into a 8 mL sealed tube, was placed a solution of tert-butyl 3-(2-[[7-(pentafluoroethyl)isoquinolin-1-yl]amino]acetamido)azetidine-1-carboxylate (as prepared in the previous step, 100 mg, 0.21 mmol, 1.00 equiv) in dichloromethane (5 mL), TFA (0.5 g). The resulting solution was stirred for 5 h at 0° C. The resulting mixture was concentrated under vacuum. The residue was washed with 3×5 mL of ether. This resulted in 0.12 g (crude) of N-(azetidin-3-yl)-2-[[7-(pentafluoroethyl)isoquinolin-1-yl]amino]acetamide as a white solid.

後処理

  1. customInto a 8 mL sealed tube
  2. concentrationThe resulting mixture was concentrated under vacuum
  3. washThe residue was washed with 3×5 mL of ether
  4. customThis resulted in 0.12 g (crude) of N-(azetidin-3-yl)-2-[[7-(pentafluoroethyl)isoquinolin-1-yl]amino]acetamide as a white solid

出典と根拠

ORDレコード
ord-b5202008192e4dc4bccf619659212041
出典データセット
uspto-grants-2013_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08518969B2

反応ノート

読み込み中…

このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート