반응 #942001

반응 방정식

7(R)-iodomethyl-2(S),3(S)-diphenyl-1,4-dioxa-spiro[4.4]nonane

1,3-dimethyl-3,4,5,6-tetrahydro-2(1H)-pyrimidinone

2-(3-chloro-4-methylsulfanyl-phenyl)-N-(2(R)-hydroxy-1 (R)-methyl-2-phenyl-ethyl)-N-methylacetamide

n-butyllithium

ammonium chloride

ammonium chloride

1,1,1,3,3,3-hexamethyldisilazane

→

2(R)-(3-chloro-4-methylsulfanyl-phenyl)-3-(2(S),3 (S)-diphenyl-1,4-dioxa-spiro [4.4]non-7(S)-yl)-N-(2(R)-hydroxy-1(R)-methyl-2-phenyl-ethyl)-N-methyl-propionamide

수율 102.1%

용매

tetrahydrofuran

toluene

tetrahydrofuran

반응 조건

후처리

1. 1
   기타the temperature below −15° C
2. 2
   기타The cold reaction mixture
3. 3
   기타the temperature below -15° C
4. 4
   온도An exotherm increased the temperature to −4° C.
5. 5
   workup.ADDITIONduring the addition
6. 6
   온도to warm to 0° C.
7. 7
   workup.STIRRINGwhere it was stirred for an additional 3 h
8. 8
   기타The organic layer was separated
9. 9
   건조The organic layer was dried over anhydrous sodium sulfate
10. 10
    농축concentrated in vacuo

실험 절차

A solution of 1,1,1,3,3,3-hexamethyldisilazane (3.18 mL, 15.05 mmol) in tetrahydrofuran (20 mL) cooled to −20° C. was treated with a 2.5M solution of n-butyllithium in hexanes (5.8 mL, 14.5 meq) over 10 min at such a rate as to keep the temperature below −15° C. The mixture was stirred for an additional 5 min. The cold reaction mixture was then treated with a solution of 2-(3-chloro-4-methylsulfanyl-phenyl)-N-(2(R)-hydroxy-1 (R)-methyl-2-phenyl-ethyl)-N-methylacetamide (prepared as in Example 30, 2.77 g, 7.61 mmol) in tetrahydrofliran (22 mL) via syringe over 8 min, at such a rate as to keep the temperature below -15° C. The reaction was then slowly allowed to warm to −7° C. over 20 min and then a solution of 7(R)-iodomethyl-2(S),3(S)-diphenyl-1,4-dioxa-spiro[4.4]nonane (2.42 g, 5.76 mmol) and 1,3-dimethyl-3,4,5,6-tetrahydro-2(1H)-pyrimidinone (1.7 mL, 14.1 mmol) in tetrahydrofuran (10 mL) was added over 6 min. An exotherm increased the temperature to −4° C. during the addition. The reaction was allowed to warm to 0° C., where it was stirred for an additional 3 h. At this time, the reaction was poured into a mixture of toluene (70 mL) and a 20% aqueous ammonium chloride solution (50 mL, 187 mmol) and was then stirred vigorously. The organic layer was separated and re-washed with a 20% aqueous ammonium chloride solution (50 mL, 187 mmol). The organic layer was dried over anhydrous sodium sulfate, and concentrated in vacuo to give 2(R)-(3-chloro-4-methylsulfanyl-phenyl)-3-(2(S),3 (S)-diphenyl-1,4-dioxa-spiro [4.4]non-7(S)-yl)-N-(2(R)-hydroxy-1(R)-methyl-2-phenyl-ethyl)-N-methyl-propionamide (3.86 g) as an overweight brown semi-solid. Flash chromatography (Merck Silica gel 60, 230-400 mesh, 1/1 hexanes/ethyl acetate) afforded 2(R)-(3-chloro-4-methylsulfanyl-phenyl)-3-(2(S),3(S)-diphenyl-1,4-dioxa-spiro[4.4]non-7(S)-yl)-N-(2(R)-hydroxy-1(R)-methyl-2-phenyl-ethyl)-N-methylpropionamide as a yellow foam (2.28 g, 60.4%).

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