참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Dicyclohexylcarbodiimide | HCID 10868 | — |
| 반응물 | 3a,4,7,7a-Tetrahydro-2-hydroxy-4,7-methano-1H-isoindole-1,3(2H)-dione | HCID 89529 | — |
| 반응물 | N-[(Phenylmethoxy)carbonyl]-L-leucylglycine | HCID 6992483 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | N,N'-Dicyclohexylurea | HCID 4277 | — |
| 생성물 | 3a,4,7,7a-Tetrahydro-2-hydroxy-4,7-methano-1H-isoindole-1,3(2H)-dione | HCID 89529 | — |
| 생성물 | N-[(Phenylmethoxy)carbonyl]-L-leucylglycine | HCID 6992483 | — |
반응 단계
A solution of the N-hydroxy-5-norbornene-2,3-dicarboximide active ester of N-benzyloxycarbonyl-L-leucylglycine was prepared according to the general procedure of M. Fujino, et al [Chem. Pharm. Bull. Japan, 22, 1857 (1974)]. A solution of 1.27 g. of N-benzyloxycarbonylleucylglycine and 0.72 g. of N-hydroxy-5-norbornene-2,3-dicarboximide in 5 ml. of tetrahydrofuran was cooled in an ice bath and 0.83 g. of N,N'-dicyclohexylcarbodiimide was added to the cold solution together with 1 ml. of tetrahydrofuran. The reaction mixture was stirred at low temperature for 40 minutes and then at room temperature for 21/2 hours. The N,N'-dicyclohexylurea formed during the reaction was collected on a filter and washed with three 1-ml. portions of tetrahydrofuran.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 특허 번호 | US04173564 |
|---|
| 출처 데이터셋 | uspto-grants-1979_11 |
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| ORD ID | ord-183450c1dc30458ca6ef56b52fe5e039 |
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| 출처 메모 | uspto-grants-1979_11 |
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