تفاعل #1583830

ord-048a0a6735ef47c49bb88bde261263f8

معادلة التفاعل

CC(C)C(=N)N.Cl
2-methyl propanimidamide hydrochloride
ClSC(Cl)(Cl)Cl
trichloromethanesulfenyl chloride
[Na+].[OH-]
sodium hydroxide
CC(C)c1nsc(Cl)n1
title compound
المردود 60.8%
CC(C)c1nsc(Cl)n1
5-chloro-3-(1-methylethyl)-1,2,4-thiadiazole
المردود 60.8%

المذيبات

ظروف التفاعل

درجة الحرارة
0°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةto warm to room temperature
  2. 2
    workup.STIRRINGstirred for an additional 3 h
  3. 3
    workup.ADDITIONIce was added to the reaction mixture
  4. 4
    أخرىthe mixture was separated
  5. 5
    استخلاصthe aqueous layer was extracted with methylene chloride (3×25 mL)
  6. 6
    تجفيفThe combined organic extracts were dried over magnesium sulfate
  7. 7
    ترشيحfiltered
  8. 8
    تركيزconcentrated under reduced pressure
  9. 9
    أخرىThe resulting residue was purified by medium pressure liquid chromatography (0 to 100% gradient of ethyl acetate in hexanes as eluant)

الإجراء التجريبي

To a mixture of 2-methyl propanimidamide hydrochloride (5.0 g, 40.8 mmol), trichloromethanesulfenyl chloride (7.14 g, 38.4 mmol) in methylene chloride (200 mL) at 0° C. was added dropwise an aqueous solution of sodium hydroxide (50%, 9.9 mL) over 20 minutes. The reaction mixture was stirred for 2 h at 0° C. and then was allowed to warm to room temperature, and stirred for an additional 3 h. Ice was added to the reaction mixture, the mixture was separated, and the aqueous layer was extracted with methylene chloride (3×25 mL). The combined organic extracts were dried over magnesium sulfate, filtered and concentrated under reduced pressure. The resulting residue was purified by medium pressure liquid chromatography (0 to 100% gradient of ethyl acetate in hexanes as eluant) to provide the title compound as a oil (3.8 g).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US09198433B2uspto-grants-2015_12