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3-benzyloxycarbonylamino-3-methyl-N-[2,3,4,5-tetrahydro-4-oxo-1H-naphtho[2,1-b]azepin-3(R)-yl]butanamide → 3-Benzyloxycarbonylamino-3-methyl-N-[2,3,4,5-tetra-hydro-4-oxo-5-[[2'-[(t-butoxycarbonylamino)methyl]-[1,1'-biphenyl]-4-yl]methyl]-1H-naphtho[2,1-b]azepin-3(R)-yl]-butanamide
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 3-benzyloxycarbonylamino-3-methyl-N-[2,3,4,5-tetrahydro-4-oxo-1H-naphtho[2,1-b]azepin-3(R)-yl]butanamide | HCID 20641421 | — |
| 反応物 | 2'-[(t-Butoxycarbonylamino)methyl]-1,1-biphenyl-4-methanol | HCID 22008472 | — |
| 生成物 | 3-Benzyloxycarbonylamino-3-methyl-N-[2,3,4,5-tetra-hydro-4-oxo-5-[[2'-[(t-butoxycarbonylamino)methyl]-[1,1'-biphenyl]-4-yl]methyl]-1H-naphtho[2,1-b]azepin-3(R)-yl]-butanamide | HCID 20641423 | — |
反応手順
The product of Step B is prepared from 3-benzyloxycarbonylamino-3-methyl-N-[2,3,4,5-tetrahydro-4-oxo-1H-naphtho[2,1-b]azepin-3(R)-yl]butanamide (Step A) and 2′-[(t-butoxycarbonylamino)methyl]-1,1′-biphenyl-4-methanol, methanesulfonate ester (Example 1, Step G) according to the procedure for Example 1, Step H.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US06211174B1 |
| 出典データセット | uspto-grants-2001_04 |
| ORD ID | ord-42dc8f2981ef4db187b6a59d56bd0aa6 |
| 出典メモ | uspto-grants-2001_04 |