تفاعل #428990
ord-61172809add7487dba30b6f3d3ca4556
معادلة التفاعل
(3RS)-3-(N-tert-butyloxycarbonylaminoethyl) pyrrolidine
N-benzyloxycarbonyl-S-methylisothiourea
KHSO4
→
title compound
(3RS)-1-(N-benzyloxycarbonylamidino)-3-aminoethyl pyrrolidine
المتفاعلات
الكواشف
لا شيء
المذيبات
ظروف التفاعل
الظروف التفصيلية
See reaction.notes.procedure_details.
المعالجة
- 1درجة الحرارةheated to 60°-70° C. for eight hours
- 2غسيلthe water layer was washed with a mixture of the toluene and ethyl acetate
- 3workup.WAITleft for 2 days under which time the Boc group
- 4أخرىwas removed
- 5استخلاصextracted four times with CH2Cl2The combined organic layer
- 6تجفيفwas dried (Na2SO4)
- 7ترشيحfiltered
- 8أخرىevaporated
الإجراء التجريبي
2.18 g (0.0102 mmole) (3RS)-3-(N-tert-butyloxycarbonylaminoethyl) pyrrolidine and 2.81 g (0.0125 mole) N-benzyloxycarbonyl-S-methylisothiourea was dissolved in 30 ml toluene and heated to 60°-70° C. for eight hours followed by stirring at room temperature for one day. 0.3M KHSO4 -solution was added and the water layer was washed with a mixture of the toluene and ethyl acetate and left for 2 days under which time the Boc group was removed. The acidic water phase was made alkaline and extracted four times with CH2Cl2The combined organic layer was dried (Na2SO4), filtered and evaporated to yield 2.0 g (51%) of the title compound.