2-tert-Butoxycarbonylamino-3-octadecylcarbamoyloxypropylamine → 2-Tert-butoxycarbonylamino-3-(3-chloropropylsulfonylamino)-1-hexadecylthiopropane
反応式
[C:1]([O:5][C:6]([NH:8]C(COC(=O)NCCCCCCCCCCCCCCCCCC)CN)=[O:7])([CH3:4])([CH3:3])[CH3:2].[Cl:35][CH2:36][CH2:37][CH2:38][S:39]([NH:42][CH2:43][CH:44](OC)[CH2:45][S:46][CH2:47][CH2:48][CH2:49][CH2:50][CH2:51][CH2:52][CH2:53][CH2:54][CH2:55][CH2:56][CH2:57][CH2:58][CH2:59][CH2:60][CH2:61][CH3:62])(=[O:41])=[O:40]>>[C:1]([O:5][C:6]([NH:8][CH:44]([CH2:43][NH:42][S:39]([CH2:38][CH2:37][CH2:36][Cl:35])(=[O:40])=[O:41])[CH2:45][S:46][CH2:47][CH2:48][CH2:49][CH2:50][CH2:51][CH2:52][CH2:53][CH2:54][CH2:55][CH2:56][CH2:57][CH2:58][CH2:59][CH2:60][CH2:61][CH3:62])=[O:7])([CH3:4])([CH3:3])[CH3:2]参加物
3
実験手順
3-Hexadecylthio-2-tert-butoxycarbonylaminopropylamine IV e4 is allowed to react and worked up by the same procedure as described in (4). m.p. 100.5°-101.5° C. The summary of the experimental condition and the physical data of the product are listed in Table 7.
後処理
- customto react
出典と根拠
- ORDレコード
- ord-3be742f95f12401e9a7b1b8f5b216bb5
- 出典データセット
- uspto-grants-1992_08
- 特許番号
- US05138067
反応ノート
読み込み中…