반응 #74560

ord-9edad214163b4510a45d7125ccc1060f

반응 방정식

Cl
HCl
N#Cc1cc(S(=O)(=O)Cl)ccc1F
3-cyano-4-fluorobenzenesulfonyl chloride
Nc1nccs1
2-aminothiazole
c1ccncc1
pyridine
N#Cc1cc(S(=O)(=O)Nc2nccs2)ccc1F
title product
수율 66.6%
N#Cc1cc(S(=O)(=O)Nc2nccs2)ccc1F
3-cyano-4-fluoro-N-(thiazol-2-yl)benzenesulfonamide
수율 66.6%

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타to give a solution
  2. 2
    workup.STIRRINGThe reaction was stirred at this temperature for 2 days
  3. 3
    기타before decanting the supernatant and
  4. 4
    농축concentrating in vacuo
  5. 5
    기타to furnish a dark oil
  6. 6
    기타the mixture triturated until solidification
  7. 7
    여과A brick red solid was filtered off
  8. 8
    세척washed with water
  9. 9
    기타dried

실험 절차

To 2-aminothiazole (12.55 g, 125.3 mmol) was added pyridine (46 ml) and dichloromethane (75 mL) and the mixture stirred to give a solution. A solution of 3-cyano-4-fluorobenzenesulfonyl chloride (25 g, 114 mmol) in dichloromethane (50 ml) was added over approx 20 minutes at room temperature. The reaction was stirred at this temperature for 2 days before decanting the supernatant and concentrating in vacuo to furnish a dark oil. 2M HCl (200 ml) was added and the mixture triturated until solidification occurred. A brick red solid was filtered off, washed with water and dried to furnish 21.5 g of the title product. 1HNMR (d6-DMSO): δ 6.9 (d, 1H), 7.3 (m, 1H), 7.6 (m, 1H), 8.15 (m, 1H), 8.3 (d, 1H), 12.9 (br s 1H). LCMS Rt=2.34 min MS m/z 284 [MH]+.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US08541588B2uspto-grants-2013_09